Canonical Allele Identifier: PA16039887
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 230215

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Gly84Val
CA032367
NM_000038.6:c.251G>T