Canonical Allele Identifier: PA2826628575
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 186209

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Ser1055Ala
CA013340
NM_001281492.2:c.3163T>G