Canonical Allele Identifier: PA2825084946
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1797439
ClinVar RCV Id: RCV002438064
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Phe10Val
CA346734511
NM_000179.3:c.28T>G