Allele Registry

Canonical Allele Identifier: PA915976036

Gene: NPHS1 HGNC NCBI

ClinVar Allele:

741814

ClinVar RCV:

RCV000905148

RCV001272290

RCV003923054

ClinVar Variation:

730355

HGVS (amino-acid)	Matching Registered Transcripts
NP_004637.1:p.Met384Thr	CA9390540 NM_004646.4:c.1151T>C