Canonical Allele Identifier: PA2827052110
Gene: SETDB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 791038
ClinVar RCV Id: RCV000973945
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001307628.1:p.Gly404Arg
CA6981936
NM_001320699.2:c.1210G>A
CA388187046
NM_001320699.2:c.1210G>C