Canonical Allele Identifier: PA101636
Gene: NDP HGNC NCBI

Linked Data

ClinVar Variation Id: 10699
ClinVar RCV Id: RCV000011445
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000257.1:p.Ser101Phe
CA255487
NM_000266.4:c.302C>T