Allele Registry

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Canonical Allele Identifier: PA658680829

Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 486904

ClinVar RCV Id: RCV000570696

ClinVar Variation Id: 1785817

ClinVar RCV Id: RCV002424129

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Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Glu699Asp	CA346750887 NM_000179.3:c.2097G>C CA346750888 NM_000179.3:c.2097G>T