Canonical Allele Identifier: PA2825160805
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2937351
ClinVar RCV Id: RCV003791541

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.Pro133Gln
CA379965781
NM_000378.6:c.398C>A