Canonical Allele Identifier: PA2828022986
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 429050
ClinVar Variation Id: 2567044
ClinVar RCV Id: RCV003278306

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Asn1384Lys
CA16032274
NM_001354906.2:c.4152T>A
CA16032275
NM_001354906.2:c.4152T>G