Canonical Allele Identifier: PA2825018149
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 966387
ClinVar RCV Id: RCV003744789
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Asp1018Gly
CA16028019
NM_000038.6:c.3053A>G