Canonical Allele Identifier: PA2827957176
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2058749
ClinVar RCV Id: RCV003744821

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Gly984Asp
CA16027713
NM_001354897.2:c.2951G>A