Canonical Allele Identifier: PA645486201
Gene: SRCAP HGNC NCBI

Linked Data

ClinVar Variation Id: 318893
ClinVar RCV Id: RCV000915066 RCV002487406 RCV003972358
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006653.2:p.Thr2374Asn
CA8012420
NM_006662.3:c.7121C>A