Canonical Allele Identifier: PA2828018869
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 3018351
ClinVar RCV Id: RCV003877014
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.His730Tyr
CA16027977
NM_001354906.2:c.2188C>T