ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2827328283
Gene: RANGRF
HGNC
NCBI
Linked Data
ClinVar Variation Id:
190841
ClinVar RCV Id:
RCV001711343
RCV001842510
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001317056.1:p.Leu18Phe
CA302117
NM_001330127.2:c.52C>T