Canonical Allele Identifier: PA2826625164
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 842691
ClinVar RCV Id: RCV001045149

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Asn177Asp
CA346740736
NM_001281492.2:c.529A>G