Canonical Allele Identifier: PA2828009156
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482516

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Pro1833Ser
CA16034417
NM_001354905.2:c.5497C>T