Canonical Allele Identifier: PA2827998937
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 489496
ClinVar RCV Id: RCV000580381

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Ser2522Thr
CA16038144
NM_001354901.2:c.7565G>C