Canonical Allele Identifier: PA645400449
Gene: RALGAPB HGNC NCBI

Linked Data

ClinVar Variation Id: 370037
ClinVar RCV Id: RCV000509009

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065069.1:p.Arg775Leu
CA9854202
NM_020336.4:c.2324G>T