Canonical Allele Identifier: PA2826631385
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 575310

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Ile443Val
CA068641
NM_001281493.2:c.1327A>G