Canonical Allele Identifier: PA2827980705
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 3231405
ClinVar RCV Id: RCV004525476

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.His2526Gln
CA16037978
NM_001354899.2:c.7578T>A
CA16037979
NM_001354899.2:c.7578T>G