Canonical Allele Identifier: PA2827962591
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470113

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Ile2625Thr
CA16038374
NM_001354897.2:c.7874T>C