Canonical Allele Identifier: PA355082
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 220176
ClinVar RCV Id: RCV000203815 RCV000561106 RCV000587117 RCV001002346 RCV003316138 RCV003997620
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.His2532Tyr
CA048637
NM_000038.6:c.7594C>T