Canonical Allele Identifier: PA2827999052
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 652208

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Asn2559Ser
CA16038396
NM_001354901.2:c.7676A>G