Canonical Allele Identifier: PA2827328287
Gene: RANGRF HGNC NCBI

Linked Data

ClinVar Variation Id: 664423
ClinVar RCV Id: RCV001842003
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317056.1:p.Met20Leu
CA397993837
NM_001330127.2:c.58A>C
CA397993842
NM_001330127.2:c.58A>T