Canonical Allele Identifier: PA2828004390
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1761528

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Ile2575Asn
CA16038702
NM_001354902.2:c.7724T>A