Canonical Allele Identifier: PA2573062132
Gene: NDP HGNC NCBI

Linked Data

ClinVar Variation Id: 1339550
ClinVar RCV Id: RCV001824259
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000257.1:p.Phe81Ser
CA413007757
NM_000266.4:c.242T>C