ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA172627
Gene: NDE1
HGNC
NCBI
Linked Data
ClinVar Variation Id:
159020
ClinVar RCV Id:
RCV000146502
RCV000764027
RCV001252592
RCV001711408
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001137451.1:p.Ser291Phe
CA172626
NM_001143979.2:c.872C>T