Canonical Allele Identifier: PA2828012437
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 664699
ClinVar RCV Id: RCV002390703 RCV004002847 RCV003537299
ClinVar Variation Id: 1759394
ClinVar RCV Id: RCV002393894
ClinVar Variation Id: 3231329
ClinVar RCV Id: RCV004525400
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Ser2352Arg
CA16037706
NM_001354905.2:c.7054A>C
CA16037712
NM_001354905.2:c.7056T>A
CA16037713
NM_001354905.2:c.7056T>G