Canonical Allele Identifier: PA203484
Gene: NPHS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 198518
ClinVar RCV Id: RCV000179892 RCV000712435 RCV001125720 RCV002294071 RCV001258315
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004637.1:p.Pro264Arg
CA203482
NM_004646.4:c.791C>G