Canonical Allele Identifier: PA645400398
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_001120982.1:p.Asn1829Ser
CA042093
NM_001127510.3:c.5486A>G