Canonical Allele Identifier: PA2825024939
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 489498

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Pro2622Thr
CA16038419
NM_000038.6:c.7864C>A