Canonical Allele Identifier: PA645400166
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411531
ClinVar RCV Id: RCV000775710 RCV002230597
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Ala1595Ser
CA16031815
NM_001127510.3:c.4783G>T