Canonical Allele Identifier: PA2827980900
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1435937
ClinVar RCV Id: RCV003772893
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Ile2587Met
CA16038376
NM_001354899.2:c.7761A>G