Canonical Allele Identifier: PA2499245069
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1189289
ClinVar RCV Id: RCV001549600
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Ser89Thr
CA346739332
NM_001281492.2:c.266G>C