Canonical Allele Identifier: PA2825024935
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 75619

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Pro2622Leu
CA16038424
NM_000038.6:c.7865C>T