Canonical Allele Identifier: PA2828002426
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2167776
ClinVar RCV Id: RCV003653675

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Asn1455Ser
CA16031491
NM_001354902.2:c.4364A>G