Canonical Allele Identifier: PA1139728054
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_057576.2:p.Pro32Leu
CA8374317
NM_016492.5:c.95C>T