Canonical Allele Identifier: PA916041598
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 141524
ClinVar RCV Id: RCV000130090 RCV000195856 RCV000485276 RCV002228483 RCV001797633 RCV003997549
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Phe2638Ile
CA014111
NM_001354896.2:c.7912T>A