Canonical Allele Identifier: PA163586
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 140800

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Asp2490Asn
CA013697
NM_001127510.3:c.7468G>A