Canonical Allele Identifier: PA330553
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89445

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ile1227Leu
CA013789
NM_000179.3:c.3679A>T
CA346760894
NM_000179.3:c.3679A>C