Canonical Allele Identifier: PA2825087436
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1767051

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Arg316Gly
CA346740797
NM_000179.3:c.946A>G