Canonical Allele Identifier: PA2741916700
Gene: NPHS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2649761
ClinVar RCV Id: RCV003415210
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004637.1:p.Pro264Leu
CA9390658
NM_004646.4:c.791C>T