Canonical Allele Identifier: PA2827995663
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 487051
ClinVar RCV Id: RCV000567763

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Ser1522Phe
CA16031733
NM_001354901.2:c.4565C>T