Canonical Allele Identifier: PA916041606
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 489499

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Asn2642Asp
CA16038432
NM_001354896.2:c.7924A>G