Canonical Allele Identifier: PA2828001367
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2092648
ClinVar RCV Id: RCV003744871
ClinVar Variation Id: 2683854
ClinVar RCV Id: RCV003484463

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Asn921Lys
CA16027973
NM_001354902.2:c.2763T>A
CA16027974
NM_001354902.2:c.2763T>G