Canonical Allele Identifier: PA16040042
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 245782

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Pro1925His
CA042917
NM_000038.6:c.5774C>A