Canonical Allele Identifier: PA2825160764
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2927916
ClinVar RCV Id: RCV003786738

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.Leu124Phe
CA379965828
NM_000378.6:c.372G>T
CA379965829
NM_000378.6:c.372G>C