ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2826128778
Gene: RANGRF
HGNC
NCBI
Linked Data
ClinVar Variation Id:
2788278
ClinVar RCV Id:
RCV003755181
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001171272.1:p.Arg59Leu
CA8374336
NM_001177801.2:c.176G>T