Canonical Allele Identifier: PA2828029699
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1761528

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Ile2565Asn
CA16038702
NM_001354903.2:c.7694T>A