Canonical Allele Identifier: PA645378700
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 233452

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ile225Met
CA10578042
NM_000179.3:c.675T>G