Canonical Allele Identifier: PA2826820996
Gene: SETD5 HGNC NCBI

Linked Data

ClinVar Variation Id: 1523969
ClinVar RCV Id: RCV002031371
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001278972.1:p.Tyr1222Cys
CA2239842
NM_001292043.1:c.3665A>G