Canonical Allele Identifier: PA2580109603
Gene: NDP HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000257.1:p.Lys58Arg
CA413008941
NM_000266.4:c.173A>G