Canonical Allele Identifier: PA2827980910
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 652208

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Asn2590Ser
CA16038396
NM_001354899.2:c.7769A>G