Canonical Allele Identifier: PA2741986815
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2927916
ClinVar RCV Id: RCV003786738
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077744.4:p.Leu124Phe
CA379965828
NM_024426.6:c.372G>T
CA379965829
NM_024426.6:c.372G>C