Canonical Allele Identifier: PA916042005
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482450
ClinVar RCV Id: RCV000572578 RCV003652019
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Asp992Tyr
CA16028117
NM_001354900.2:c.2974G>T