Canonical Allele Identifier: PA2580307033
Gene: NPHS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2032904
ClinVar RCV Id: RCV002885067
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004637.1:p.Asp310Tyr
CA405406796
NM_004646.4:c.928G>T