Canonical Allele Identifier: PA2826128758
Gene: RANGRF HGNC NCBI

Linked Data

ClinVar Variation Id: 1110143
ClinVar RCV Id: RCV001842032 RCV003946140
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171272.1:p.Val42Leu
CA8374322
NM_001177801.2:c.124G>T
CA397994093
NM_001177801.2:c.124G>C