Canonical Allele Identifier: PA2826128761
Gene: RANGRF HGNC NCBI

Linked Data

ClinVar Variation Id: 288027
ClinVar RCV Id: RCV000376329 RCV001843040
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171272.1:p.Asp44Glu
CA8374325
NM_001177801.2:c.132C>A
CA397994144
NM_001177801.2:c.132C>G