Canonical Allele Identifier: PA16040032
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_000029.2:p.Ser1842Thr
CA042221
NM_000038.6:c.5524T>A