Canonical Allele Identifier: PA2827329909
Gene: RAB11FIP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2392190
ClinVar RCV Id: RCV004225621
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317096.1:p.Trp332Arg
CA378567259
NM_001330167.2:c.994T>C
CA378567260
NM_001330167.2:c.994T>A