Canonical Allele Identifier: PA2826626636
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 578926
ClinVar RCV Id: RCV000702075
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Gly522Glu
CA346750571
NM_001281492.2:c.1565G>A