Canonical Allele Identifier: PA1139741884
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_001341825.1:p.Ile2633Leu
CA16038371
NM_001354896.2:c.7897A>C
CA16038372
NM_001354896.2:c.7897A>T