Canonical Allele Identifier: PA2827957296
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181776

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Asn1027del
CA008002
NM_001354897.2:c.3079_3081del