Canonical Allele Identifier: PA286657
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 127313
ClinVar RCV Id: RCV000115112 RCV000122792 RCV000235096 RCV000587692 RCV003398710 RCV003743565 RCV003997227
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Pro2158Arg
CA012210
NM_001127510.3:c.6473C>G