Canonical Allele Identifier: PA916041601
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 489498

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Pro2640Thr
CA16038419
NM_001354896.2:c.7918C>A