Canonical Allele Identifier: PA2830002174
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2926856
ClinVar RCV Id: RCV003789094

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077744.4:p.Met302Ile
CA379962181
NM_024426.6:c.906G>T
CA379962182
NM_024426.6:c.906G>C
CA379962183
NM_024426.6:c.906G>A