Canonical Allele Identifier: PA2827980908
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 216181

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Asn2590Asp
CA338662
NM_001354899.2:c.7768A>G