Canonical Allele Identifier: PA2827980018
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1336346

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Pro2318Leu
CA16036672
NM_001354899.2:c.6953C>T