Canonical Allele Identifier: PA2825085037
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1429804
ClinVar RCV Id: RCV001939118 RCV002425270
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ser28Ala
CA346734802
NM_000179.3:c.82T>G