Allele Registry

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Canonical Allele Identifier: PA658680044

Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 483775

ClinVar RCV Id: RCV000562024 RCV000629755 RCV000759848 RCV004001048

ClinVar Variation Id: 926791

ClinVar RCV Id: RCV001189602 RCV001192489 RCV002560057

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Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Ser63Ala	CA346735021 NM_000179.3:c.187T>G CA1139655608 NM_000179.3:c.186_187delinsAG