Canonical Allele Identifier: PA2827692873
Gene: SCAPER HGNC NCBI

Linked Data

ClinVar Variation Id: 427855
ClinVar RCV Id: RCV000523592 RCV000722056
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339940.1:p.Ser1091Asn
CA393520110
NM_001353011.1:c.3272G>A