Canonical Allele Identifier: PA346570
Gene: NPHS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 180464
ClinVar RCV Id: RCV000157400 RCV000354078 RCV000879498 RCV002294058 RCV001094540
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004637.1:p.Gly601Ala
CA346568
NM_004646.4:c.1802G>C