ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2826128779
Gene: RANGRF
HGNC
NCBI
Linked Data
ClinVar Variation Id:
1403512
ClinVar RCV Id:
RCV001909093
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001171272.1:p.Arg59Pro
CA397994394
NM_001177801.2:c.176G>C