Canonical Allele Identifier: PA2828013139
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1052468
ClinVar RCV Id: RCV003771065
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Ser2467Ala
CA16038452
NM_001354905.2:c.7399T>G