Canonical Allele Identifier: PA658807701
Gene: SETD2 HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_054878.5:p.Lys941Arg
CA352525019
NM_014159.7:c.2822A>G