Canonical Allele Identifier: PA2827692769
Gene: SCAPER HGNC NCBI

Linked Data

ClinVar Variation Id: 427855
ClinVar RCV Id: RCV000523592 RCV000722056
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339939.1:p.Ser1085Asn
CA393520110
NM_001353010.1:c.3254G>A