Canonical Allele Identifier: PA2827980927
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 489498

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Pro2594Thr
CA16038419
NM_001354899.2:c.7780C>A