Canonical Allele Identifier: PA2828021728
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411419

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Pro1184Ser
CA038968
NM_001354906.2:c.3550C>T