Canonical Allele Identifier: PA2826628785
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 849724
ClinVar RCV Id: RCV001053749
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Val1101Ala
CA346760964
NM_001281492.2:c.3302T>C