Canonical Allele Identifier: PA2826625794
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 142181
ClinVar RCV Id: RCV000131161 RCV000196009 RCV000409980 RCV000524107 RCV000590712 RCV001355650 RCV002281960
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Asn325Thr
CA008530
NM_001281492.2:c.974A>C