Canonical Allele Identifier: PA174781
Gene: RAB11FIP4 HGNC NCBI

Linked Data

ClinVar Variation Id: 161785
ClinVar RCV Id: RCV000149321

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_116321.2:p.Glu634Val
CA174780
NM_032932.6:c.1901A>T