Canonical Allele Identifier: PA2826624767
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1974899
ClinVar RCV Id: RCV002746344
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Pro59Leu
CA346735005
NM_001281492.2:c.176C>T