Canonical Allele Identifier: PA2825160598
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 663192
ClinVar RCV Id: RCV000821019 RCV002501137 RCV003467502
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.Gly75Ser
CA064759
NM_000378.6:c.223G>A