Canonical Allele Identifier: PA2825644700
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 489498

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Pro2604Thr
CA16038419
NM_001127511.3:c.7810C>A