Canonical Allele Identifier: PA2827956388
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 566805

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Lys748Arg
CA16026181
NM_001354897.2:c.2243A>G