Canonical Allele Identifier: PA2828084232
Gene: RBM48 HGNC NCBI

Linked Data

ClinVar Variation Id: 1435189
ClinVar RCV Id: RCV001984820
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350295.1:p.Arg24Trp
CA161982375
NM_001363366.1:c.70C>T