Canonical Allele Identifier: PA2826222605
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2926856
ClinVar RCV Id: RCV003789094
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001185480.1:p.Met85Ile
CA379962181
NM_001198551.1:c.255G>T
CA379962182
NM_001198551.1:c.255G>C
CA379962183
NM_001198551.1:c.255G>A