Canonical Allele Identifier: PA2825634040
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1018219
ClinVar RCV Id: RCV002543727

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Asn1981Lys
CA16034338
NM_001127510.3:c.5943T>A
CA16034339
NM_001127510.3:c.5943T>G