Canonical Allele Identifier: PA2826627108
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 935359
ClinVar RCV Id: RCV001203930 RCV002307698 RCV004010633
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Val632Ile
CA346752910
NM_001281492.2:c.1894G>A