Canonical Allele Identifier: PA2828018908
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1042543
ClinVar RCV Id: RCV002242366
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Asp735Tyr
CA16028017
NM_001354906.2:c.2203G>T