Canonical Allele Identifier: PA2825160449
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2928142
ClinVar RCV Id: RCV003786964
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.Gln35His
CA219511452
NM_000378.6:c.105G>T
CA379966374
NM_000378.6:c.105G>C