Canonical Allele Identifier: PA645375263
Gene: NPHS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 328877
ClinVar RCV Id: RCV000407307
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004637.1:p.Pro169Thr
CA10652380
NM_004646.4:c.505C>A