Canonical Allele Identifier: PA2580307026
Gene: NPHS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2148753
ClinVar RCV Id: RCV003063551 RCV003906475
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004637.1:p.Val266Met
CA9390653
NM_004646.4:c.796G>A