Canonical Allele Identifier: PA2827946352
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 185017

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.His2149Pro
CA011185
NM_001354895.2:c.6446A>C