Canonical Allele Identifier: PA2580109632
Gene: NDP HGNC NCBI

Linked Data

ClinVar Variation Id: 2138557
ClinVar RCV Id: RCV003041442
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000257.1:p.Pro98Arg
CA413007511
NM_000266.4:c.293C>G