Canonical Allele Identifier: PA330555
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89446
ClinVar RCV Id: RCV000491032 RCV001355101
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ala1228Pro
CA013799
NM_000179.3:c.3682G>C