Canonical Allele Identifier: PA2827970900
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2082323
ClinVar RCV Id: RCV003534924
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Met2339Val
CA046864
NM_001354898.2:c.7015A>G