Canonical Allele Identifier: PA2826586962
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 525677
ClinVar RCV Id: RCV000629856

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Val1010Leu
CA346761488
NM_001281494.2:c.3028G>C