Canonical Allele Identifier: PA1139673118
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 935156

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Glu446Lys
CA346744558
NM_000179.3:c.1336G>A