Canonical Allele Identifier: PA645486261
Gene: SRCAP HGNC NCBI

Linked Data

ClinVar Variation Id: 318905
ClinVar RCV Id: RCV000334801 RCV001850689 RCV002521008
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006653.2:p.Gly2834Arg
CA8012713
NM_006662.3:c.8500G>A
CA395637861
NM_006662.3:c.8500G>C