Canonical Allele Identifier: PA2826625151
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 927069
ClinVar RCV Id: RCV001190080
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Met173Val
CA346740712
NM_001281492.2:c.517A>G