Canonical Allele Identifier: PA2827942282
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 485127

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.His913Arg
CA033216
NM_001354895.2:c.2738A>G