Canonical Allele Identifier: PA097049
Gene: NPHS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 56507
ClinVar RCV Id: RCV000049920 RCV001003825
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004637.1:p.Pro167Leu
CA250243
NM_004646.4:c.500C>T