Canonical Allele Identifier: PA2825665701
Gene: NPHP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 330737
ClinVar RCV Id: RCV000264341 RCV000321777 RCV000366304
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121651.1:p.Asn136Ser
CA10611788
NM_001128179.3:c.407A>G