Canonical Allele Identifier: PA2741813893
Gene: NDP HGNC NCBI

Linked Data

ClinVar Variation Id: 2663356
ClinVar RCV Id: RCV003442544
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000257.1:p.Cys55Ser
CA413008962
NM_000266.4:c.164G>C
CA413008964
NM_000266.4:c.163T>A