Canonical Allele Identifier: PA2825085067
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 3073211
ClinVar RCV Id: RCV004015225

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Gly32Arg
CA346734826
NM_000179.3:c.94G>C