Allele Registry

Canonical Allele Identifier: PA645375181

Gene: NPHS1 HGNC NCBI

ClinVar RCV:

RCV000490334

RCV000903298

RCV002271466

ClinVar Variation:

225424

HGVS (amino-acid)	Matching Registered Transcripts
NP_004637.1:p.Ala22Val	CA9390924 NM_004646.4:c.65C>T