Canonical Allele Identifier: PA916011058
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_001268421.1:p.Ser63Ala
CA346735021
NM_001281492.2:c.187T>G
CA1139655608
NM_001281492.2:c.186_187delinsAG