Canonical Allele Identifier: PA2825536016
Gene: NIPAL4 HGNC NCBI

Linked Data

ClinVar Variation Id: 3200163
ClinVar RCV Id: RCV004493063
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092757.2:p.Ser67Arg
CA361980229
NM_001099287.2:c.199A>C
CA361980235
NM_001099287.2:c.201C>G
CA361980236
NM_001099287.2:c.201C>A