Canonical Allele Identifier: PA2826632243
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 237168

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Ile642Val
CA10582071
NM_001281493.2:c.1924A>G