Canonical Allele Identifier: PA645379256
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 428385

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Lys317Glu
CA346740815
NM_000179.3:c.949A>G