Canonical Allele Identifier: PA916040682
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 419113
ClinVar RCV Id: RCV000483629 RCV000491516 RCV001731707 RCV004002286 RCV003766666
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Asn1847Ser
CA042093
NM_001354896.2:c.5540A>G