Canonical Allele Identifier: PA2828025630
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470038

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Pro1803Ala
CA044235
NM_001354906.2:c.5407C>G