Canonical Allele Identifier: PA645381225
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 231915
ClinVar RCV Id: RCV000214027
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Val653Ala
CA10578089
NM_000179.3:c.1958T>C