Canonical Allele Identifier: PA2741813892
Gene: NDP HGNC NCBI

Linked Data

ClinVar Variation Id: 2833339
ClinVar RCV Id: RCV003691940
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000257.1:p.Tyr53His
CA10391438
NM_000266.4:c.157T>C