Canonical Allele Identifier: PA2828029107
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1716653
ClinVar RCV Id: RCV003743860

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Ser2474Tyr
CA16038105
NM_001354903.2:c.7421C>A