Canonical Allele Identifier: PA2580307028
Gene: NPHS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2099614
ClinVar RCV Id: RCV003023091
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004637.1:p.Gly270Arg
CA405407057
NM_004646.4:c.808G>C