Canonical Allele Identifier: PA096930
Gene: NPHS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 56523
ClinVar RCV Id: RCV000049936 RCV003320551
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004637.1:p.Gly270Cys
CA250275
NM_004646.4:c.808G>T