Canonical Allele Identifier: PA2828001008
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 41499
ClinVar RCV Id: RCV000034381 RCV000162586 RCV001268977 RCV003650353
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Asn722Ser
CA007470
NM_001354902.2:c.2165A>G