Canonical Allele Identifier: PA2825536011
Gene: NIPAL4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2377450
ClinVar RCV Id: RCV002674053 RCV003561157
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092757.2:p.Ser39Arg
CA3534530
NM_001099287.2:c.117C>A
CA361980002
NM_001099287.2:c.115A>C
CA361980015
NM_001099287.2:c.117C>G