Canonical Allele Identifier: PA2828007588
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 926382
ClinVar RCV Id: RCV001188974
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Ala1558Val
CA16032596
NM_001354905.2:c.4673C>T