Canonical Allele Identifier: PA2828029318
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2773166
ClinVar RCV Id: RCV003538351

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Ser2506Tyr
CA16038321
NM_001354903.2:c.7517C>A