Canonical Allele Identifier: PA2827989980
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_001341829.1:p.Ile2574Leu
CA16038371
NM_001354900.2:c.7720A>C
CA16038372
NM_001354900.2:c.7720A>T