Canonical Allele Identifier: PA2825021632
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 423629

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Gly1767Asp
CA16032918
NM_000038.6:c.5300G>A