Canonical Allele Identifier: PA915963552
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 656029
ClinVar RCV Id: RCV000812334
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Leu290Arg
CA346740628
NM_000179.3:c.869T>G