Canonical Allele Identifier: PA2825089112
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2817259
ClinVar RCV Id: RCV003760929

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Gly674Ala
CA346750703
NM_000179.3:c.2021G>C