Canonical Allele Identifier: PA097130
Gene: NPHS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 56420
ClinVar RCV Id: RCV000049833 RCV001065065
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004637.1:p.Ser366Arg
CA250085
NM_004646.4:c.1096A>C
CA405406420
NM_004646.4:c.1098T>G
CA405406421
NM_004646.4:c.1098T>A