Allele Registry

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Canonical Allele Identifier: PA2826128750

Gene: RANGRF HGNC NCBI

Linked Data

ClinVar Variation Id: 2273252

ClinVar RCV Id: RCV004124096

JSON-LD

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001171272.1:p.Ser26Arg	CA397993916 NM_001177801.2:c.76A>C CA397993972 NM_001177801.2:c.78C>A CA397993974 NM_001177801.2:c.78C>G