Canonical Allele Identifier: PA16040123
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 233218

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Leu2493Pro
CA048192
NM_000038.6:c.7478T>C