Canonical Allele Identifier: PA101373
Gene: NDP HGNC NCBI
ClinVar RCV:
RCV000011431
ClinVar Variation:
10685
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000257.1:p.Cys69Ser
CA255472
NM_000266.4:c.206G>C
CA413007941
NM_000266.4:c.205T>A