Canonical Allele Identifier: PA2741833863
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_001120983.2:p.His995Tyr
CA16027977
NM_001127511.3:c.2983C>T