Canonical Allele Identifier: PA2827961782
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2907983
ClinVar RCV Id: RCV003651671

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Gly2380Asp
CA16036812
NM_001354897.2:c.7139G>A