ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2826128873
Gene: RANGRF
HGNC
NCBI
Linked Data
ClinVar Variation Id:
2157756
ClinVar RCV Id:
RCV003079660
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001171273.1:p.Ala64Thr
CA8374341
NM_001177802.2:c.190G>A