Canonical Allele Identifier: PA2827941708
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 469735

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Ala740Thr
CA16026193
NM_001354895.2:c.2218G>A