Canonical Allele Identifier: PA16040011
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 232982

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Gly1721Asp
CA10578397
NM_000038.6:c.5162G>A