Canonical Allele Identifier: PA2827998108
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 826747
ClinVar Variation Id: 1320686

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Asn2268Lys
CA16036550
NM_001354901.2:c.6804C>A
CA16036551
NM_001354901.2:c.6804C>G