Canonical Allele Identifier: PA2826631047
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1784014
ClinVar RCV Id: RCV002416951
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Glu363Lys
CA346750652
NM_001281493.2:c.1087G>A