Canonical Allele Identifier: PA2828012008
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 229765
ClinVar RCV Id: RCV000216831 RCV003650472
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Pro2380Leu
CA10578443
NM_001354902.2:c.7139C>T