Canonical Allele Identifier: PA2827495658
Gene: SETD5 HGNC NCBI

Linked Data

ClinVar Variation Id: 1803640
ClinVar RCV Id: RCV002467310
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001336380.1:p.[Thr1210_Ser1212delinsHis;Ala1214_Thr1217delinsArg]
CA2580070740
NM_001349451.2:c.3628_3650delinsCATTTACG