Canonical Allele Identifier: PA2826627219
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2761044
ClinVar RCV Id: RCV003594383

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Tyr656Cys
CA346753585
NM_001281492.2:c.1967A>G