Canonical Allele Identifier: PA2828047931
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 433676

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Pro2383Ser
CA16037691
NM_001354904.2:c.7147C>T