Canonical Allele Identifier: PA2827971761
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1760974

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Asn2599Lys
CA16038436
NM_001354898.2:c.7797T>A
CA16038437
NM_001354898.2:c.7797T>G