Canonical Allele Identifier: PA658803666
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 537485

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Gly524Asp
CA028449
NM_001127510.3:c.1571G>A