Canonical Allele Identifier: PA2573086186
Gene: NPHS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1339085
ClinVar RCV Id: RCV001823539 RCV001869816
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004637.1:p.Cys265Ser
CA9390655
NM_004646.4:c.794G>C
CA405407084
NM_004646.4:c.793T>A