Canonical Allele Identifier: PA2828004367
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 495374

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Asp2565Gly
CA16038634
NM_001354902.2:c.7694A>G