Canonical Allele Identifier: PA2826634879
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 843363
ClinVar RCV Id: RCV001045971 RCV002393226
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Val206Met
CA067797
NM_001281494.2:c.616G>A