Canonical Allele Identifier: PA2827980558
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 433676

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Pro2481Ser
CA16037691
NM_001354899.2:c.7441C>T