Canonical Allele Identifier: PA16040016
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 236616

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Ala1755Val
CA041104
NM_000038.6:c.5264C>T