Canonical Allele Identifier: PA162055
Gene: SETD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 135220
ClinVar RCV Id: RCV000122032 RCV000428574 RCV001087250
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_054878.5:p.Pro751Thr
CA162053
NM_014159.7:c.2251C>A