Canonical Allele Identifier: PA2825092105
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2129084
ClinVar RCV Id: RCV003057901

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Glu1234Asp
CA346760982
NM_000179.3:c.3702A>C
CA346760983
NM_000179.3:c.3702A>T