Canonical Allele Identifier: PA2827958900
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 141521

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Thr1503Met
CA009574
NM_001354897.2:c.4508C>T