Canonical Allele Identifier: PA2827962181
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 140800

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Asp2500Asn
CA013697
NM_001354897.2:c.7498G>A