Canonical Allele Identifier: PA166779
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 141916
ClinVar RCV Id: RCV000130625 RCV000589175 RCV001086478 RCV001260255 RCV003998071
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Pro1278Thr
CA014466
NM_000179.3:c.3832C>A