Canonical Allele Identifier: PA2580136039
Gene: SETD5 HGNC NCBI

Linked Data

ClinVar Variation Id: 2052701
ClinVar RCV Id: RCV002937646
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073986.1:p.Leu1294Val
CA351691952
NM_001080517.3:c.3880C>G