Canonical Allele Identifier: PA916040695
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 232546
ClinVar RCV Id: RCV000215089 RCV000235925 RCV000271229 RCV002515673 RCV003997982 RCV003947727
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Ser1860Thr
CA042221
NM_001354896.2:c.5578T>A