Canonical Allele Identifier: PA2827971749
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 489498

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Pro2597Thr
CA16038419
NM_001354898.2:c.7789C>A