Canonical Allele Identifier: PA206917
Gene: SRCAP HGNC NCBI

Linked Data

ClinVar Variation Id: 212301
ClinVar RCV Id: RCV000193429 RCV002492882 RCV002517138
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006653.2:p.Ser2576del
CA206916
NM_006662.3:c.7725_7727del