Canonical Allele Identifier: PA2826624930
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 230454

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Ser122Ala
CA073439
NM_001281492.2:c.364T>G