Canonical Allele Identifier: PA2827999086
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 827304
ClinVar RCV Id: RCV001026900 RCV001354620 RCV003153893 RCV003744725
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Ser2568Thr
CA16038450
NM_001354901.2:c.7702T>A