Canonical Allele Identifier: PA2826627179
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2587343
ClinVar RCV Id: RCV003360821

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Leu648Pro
CA346753385
NM_001281492.2:c.1943T>C