Canonical Allele Identifier: PA2828011960
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 236643
ClinVar RCV Id: RCV000484267 RCV000776318 RCV003650538 RCV002516295 RCV003998688
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Ser2373Tyr
CA047889
NM_001354902.2:c.7118C>A