ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA095485
Gene: NPHS2
HGNC
NCBI
Linked Data
ClinVar Variation Id:
447882
ClinVar RCV Id:
RCV000517167
RCV000761450
RCV001273612
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_055440.1:p.Val260Glu
CA1267132
NM_014625.4:c.779T>A