Canonical Allele Identifier: PA2741850328
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2567495
ClinVar RCV Id: RCV003278534

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Thr82Arg
CA346739232
NM_001281492.2:c.245C>G