Canonical Allele Identifier: PA2827950764
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_001341825.1:p.Asn1030Lys
CA16027973
NM_001354896.2:c.3090T>A
CA16027974
NM_001354896.2:c.3090T>G