Canonical Allele Identifier: PA2826128842
Gene: RANGRF HGNC NCBI

Linked Data

ClinVar Variation Id: 956645
ClinVar RCV Id: RCV001841190
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171273.1:p.Pro32Leu
CA8374317
NM_001177802.2:c.95C>T