Canonical Allele Identifier: PA916040252
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411419

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Pro1485Ser
CA038968
NM_001354896.2:c.4453C>T