Canonical Allele Identifier: PA096838
Gene: NPHS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 56458
ClinVar RCV Id: RCV000049871
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004637.1:p.Asn673Lys
CA250161
NM_004646.4:c.2019C>A
CA9390258
NM_004646.4:c.2019C>G