Canonical Allele Identifier: PA215496
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 41520
ClinVar RCV Id: RCV000034405 RCV000131638 RCV000211900 RCV000987559 RCV001154528 RCV001353623 RCV003996159 RCV003743548
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Ile544Thr
CA005403
NM_001127510.3:c.1631T>C