Canonical Allele Identifier: PA2827997145
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 485114

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Asp1977Asn
CA16034696
NM_001354901.2:c.5929G>A