Canonical Allele Identifier: PA2828001788
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 133509
ClinVar RCV Id: RCV000120014 RCV000131570 RCV000199645 RCV000587732 RCV003315713 RCV003743572
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Asn1126Thr
CA008605
NM_001354902.2:c.3377A>C