Canonical Allele Identifier: PA2828004391
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1761613

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Asn2577del
CA2580072453
NM_001354902.2:c.7728_7730del