Canonical Allele Identifier: PA1139680837
Gene: NDP HGNC NCBI

Linked Data

ClinVar Variation Id: 985284
ClinVar RCV Id: RCV001266110
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000257.1:p.Lys86Asn
CA413007652
NM_000266.4:c.258G>T
CA413007653
NM_000266.4:c.258G>C