Canonical Allele Identifier: PA2825644314
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482396

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Met2473Ile
CA16037587
NM_001127511.3:c.7419G>A
CA16037588
NM_001127511.3:c.7419G>C
CA16037589
NM_001127511.3:c.7419G>T