Canonical Allele Identifier: PA2825160549
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1518459
ClinVar RCV Id: RCV002021760
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.Gln59His
CA379966222
NM_000378.6:c.177G>T
CA379966223
NM_000378.6:c.177G>C