Canonical Allele Identifier: PA2828084270
Gene: RBM48 HGNC NCBI

Linked Data

ClinVar Variation Id: 2050924
ClinVar RCV Id: RCV002922154
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350296.1:p.Ile141Met
CA161987317
NM_001363367.1:c.423C>G