Canonical Allele Identifier: PA2828001544
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411388

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Ala1016Ser
CA16028614
NM_001354902.2:c.3046G>T