Canonical Allele Identifier: PA2827998648
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 233218

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Leu2434Pro
CA048192
NM_001354901.2:c.7301T>C