Canonical Allele Identifier: PA2830056062
Gene: RBM48 HGNC NCBI
ClinVar RCV:
RCV002923179
ClinVar Variation:
2057097
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115496.2:p.Cys180Arg
CA4341892
NM_032120.3:c.538T>C