Canonical Allele Identifier: PA2827998705
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 231400

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Asn2451Ser
CA10578446
NM_001354901.2:c.7352A>G