Canonical Allele Identifier: PA2828007732
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 489466
ClinVar RCV Id: RCV000580755 RCV003767263
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Arg1582Leu
CA16032754
NM_001354905.2:c.4745G>T