Canonical Allele Identifier: PA2580519713
Gene: SLFN13 HGNC NCBI

Linked Data

ClinVar Variation Id: 2400491
ClinVar RCV Id: RCV004236295
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_653283.3:p.Ala353Ser
CA8503894
NM_144682.6:c.1057G>T