Canonical Allele Identifier: PA2828686268
Gene: SRSF12 HGNC NCBI

Linked Data

ClinVar Variation Id: 3170257
ClinVar RCV Id: RCV004460687
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001363827.1:p.His154Leu
CA364944378
NM_001376898.1:c.461A>T