Canonical Allele Identifier: PA2827944897
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1511823
ClinVar RCV Id: RCV003773416

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Ala1700Gly
CA16032481
NM_001354895.2:c.5099C>G