Canonical Allele Identifier: PA2826631378
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1788028
ClinVar RCV Id: RCV002428173
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Leu441Trp
CA346752486
NM_001281493.2:c.1322T>G