Canonical Allele Identifier: PA1139672776
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 928121
ClinVar RCV Id: RCV001191780

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ile329Val
CA346741067
NM_000179.3:c.985A>G