Canonical Allele Identifier: PA2827947496
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482396

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Met2491Ile
CA16037587
NM_001354895.2:c.7473G>A
CA16037588
NM_001354895.2:c.7473G>C
CA16037589
NM_001354895.2:c.7473G>T