Canonical Allele Identifier: PA2580232421
Gene: RBM48 HGNC NCBI

Linked Data

ClinVar Variation Id: 2057097
ClinVar RCV Id: RCV002923179
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350296.1:p.Cys5Arg
CA4341892
NM_001363367.1:c.13T>C