Canonical Allele Identifier: PA2826633942
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 525677
ClinVar RCV Id: RCV000629856
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Val1010Leu
CA346761488
NM_001281493.2:c.3028G>C