Canonical Allele Identifier: PA658662832
Gene: NPHS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 447877
ClinVar RCV Id: RCV000517708 RCV000888629 RCV003343885
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055440.1:p.Ala61Val
CA1267300
NM_014625.4:c.182C>T