Canonical Allele Identifier: PA2828014479
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411498
ClinVar RCV Id: RCV000460219 RCV000570515 RCV000483019 RCV003651878
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Ser16Thr
CA051068
NM_001354906.2:c.46T>A