Canonical Allele Identifier: PA190791
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 185017

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.His2149Pro
CA011185
NM_000038.6:c.6446A>C