Canonical Allele Identifier: PA168638
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89476
ClinVar RCV Id: RCV000131709 RCV000454725 RCV000662523 RCV000759868 RCV001082428 RCV001357732 RCV003448259 RCV003492403
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Thr1284Met
CA014580
NM_000179.3:c.3851C>T