Canonical Allele Identifier: PA2826626697
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1784018
ClinVar RCV Id: RCV002416955
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Glu535Gln
CA346750653
NM_001281492.2:c.1603G>C