Canonical Allele Identifier: PA2826631415
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1788513
ClinVar RCV Id: RCV002443622

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Gly450Val
CA346752709
NM_001281493.2:c.1349G>T