Canonical Allele Identifier: PA2827989837
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2413101
ClinVar RCV Id: RCV003110116

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Ser2530Pro
CA16038081
NM_001354900.2:c.7588T>C