Canonical Allele Identifier: PA358899
Gene: SLFN14 HGNC NCBI

Linked Data

ClinVar Variation Id: 225535
ClinVar RCV Id: RCV000210920 RCV001267345
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123292.1:p.Lys218Glu
CA358898
NM_001129820.2:c.652A>G