Canonical Allele Identifier: PA2827990121
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 489501
ClinVar RCV Id: RCV000580553

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Asp2615Asn
CA16038630
NM_001354900.2:c.7843G>A