Canonical Allele Identifier: PA2828007855
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 236617

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Asn1601Thr
CA10582324
NM_001354905.2:c.4802A>C