Canonical Allele Identifier: PA658675280
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_065894.2:p.Ser1219Asn
CA393520110
NM_020843.2:c.3656G>A