Canonical Allele Identifier: PA916011266
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 428405
ClinVar RCV Id: RCV000490990 RCV000659893 RCV001865529 RCV000521749
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Met903Lys
CA346756599
NM_001281492.2:c.2708T>A