Canonical Allele Identifier: PA096701
Gene: NPHS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 56522
ClinVar RCV Id: RCV000049935 RCV000996847 RCV002281898
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004637.1:p.Arg256Trp
CA250273
NM_004646.4:c.766C>T