Canonical Allele Identifier: PA2828004420
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1317229
ClinVar RCV Id: RCV001759101
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Ile2592Ser
CA16038805
NM_001354902.2:c.7775T>G