Canonical Allele Identifier: PA337668
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 216325

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Gly32Cys
CA073625
NM_000179.3:c.94G>T