Canonical Allele Identifier: PA174853
Gene: GPR26 HGNC NCBI

Linked Data

ClinVar Variation Id: 161823
ClinVar RCV Id: RCV000149359
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_703143.1:p.Ala24Val
CA174852
NM_153442.4:c.71C>T