Canonical Allele Identifier: PA2826674103
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_001269847.1:p.Arg771Leu
CA9854202
NM_001282918.2:c.2312G>T