Canonical Allele Identifier: PA2825085137
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1058623
ClinVar RCV Id: RCV001367783
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Pro38His
CA346734856
NM_000179.3:c.113C>A