Canonical Allele Identifier: PA16040077
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 233045

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Ala2128Val
CA044469
NM_000038.6:c.6383C>T