Canonical Allele Identifier: PA2580109624
Gene: NDP HGNC NCBI

Linked Data

ClinVar Variation Id: 1701597
ClinVar RCV Id: RCV002276470
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000257.1:p.Cys93Tyr
CA413007568
NM_000266.4:c.278G>A
CA2580100956
NM_000266.4:c.276_278delinsATA