Canonical Allele Identifier: PA2580136078
Gene: SETD5 HGNC NCBI

Linked Data

ClinVar Variation Id: 1702955
ClinVar RCV Id: RCV002279868
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073986.1:p.Arg1338Ser
CA351693707
NM_001080517.3:c.4014G>C
CA351693710
NM_001080517.3:c.4014G>T