Canonical Allele Identifier: PA2828034531
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 566805

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Lys612Arg
CA16026181
NM_001354904.2:c.1835A>G