Canonical Allele Identifier: PA2828686262
Gene: SRSF12 HGNC NCBI
ClinVar RCV:
RCV004460687
ClinVar Variation:
3170257
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001363826.1:p.His154Leu
CA364944378
NM_001376897.1:c.461A>T