Canonical Allele Identifier: PA097095
Gene: NPHS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 56442
ClinVar RCV Id: RCV000049855 RCV002513691
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004637.1:p.Pro519Ser
CA250125
NM_004646.4:c.1555C>T