Canonical Allele Identifier: PA645375174
Gene: NPHS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 259502
ClinVar RCV Id: RCV000244392 RCV000669644 RCV000904912 RCV001124814
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004637.1:p.Gly15Arg
CA9390942
NM_004646.4:c.43G>C
CA405412624
NM_004646.4:c.43G>A