Canonical Allele Identifier: PA916041602
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 75619

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Pro2640Leu
CA16038424
NM_001354896.2:c.7919C>T