Canonical Allele Identifier: PA2828023596
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 236617

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Asn1478Thr
CA10582324
NM_001354906.2:c.4433A>C