Canonical Allele Identifier: PA2828029237
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 941020
ClinVar Variation Id: 2452683
ClinVar RCV Id: RCV003177457

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Ile2332Leu
CA16038371
NM_001354906.2:c.6994A>C
CA16038372
NM_001354906.2:c.6994A>T