Canonical Allele Identifier: PA2827970896
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482469

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Gly2337Ala
CA16036765
NM_001354898.2:c.7010G>C