Canonical Allele Identifier: PA2826674038
Gene: RALGAPB HGNC NCBI

Linked Data

ClinVar Variation Id: 370037
ClinVar RCV Id: RCV000509009
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269846.1:p.Arg775Leu
CA9854202
NM_001282917.2:c.2324G>T