Canonical Allele Identifier: PA658804798
Gene: NPHP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 501727
ClinVar RCV Id: RCV000594034 RCV000638098 RCV004543376
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000263.2:p.Ile529Met
CA1827026
NM_000272.5:c.1587A>G