Canonical Allele Identifier: PA2826624920
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1759055
ClinVar RCV Id: RCV002391461
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Arg119Met
CA073430
NM_001281492.2:c.356G>T