Canonical Allele Identifier: PA2828000594
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 490227
ClinVar RCV Id: RCV000583720 RCV001755969 RCV003744589
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Ala513Val
CA16025286
NM_001354902.2:c.1538C>T