Canonical Allele Identifier: PA190034
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 184781
ClinVar Variation Id: 643969

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Met303Ile
CA016648
NM_000179.3:c.909G>T
CA346740716
NM_000179.3:c.909G>A
CA346740717
NM_000179.3:c.909G>C