Canonical Allele Identifier: PA915975986
Gene: NPHS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 724178
ClinVar RCV Id: RCV000898050 RCV001125719 RCV001272296 RCV001796311 RCV002294410
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004637.1:p.Arg268Gln
CA9390651
NM_004646.4:c.803G>A