Canonical Allele Identifier: PA2825642059
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 236617

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Asn1743Thr
CA10582324
NM_001127511.3:c.5228A>C