Canonical Allele Identifier: PA2825160393
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 860998
ClinVar RCV Id: RCV001067413 RCV004000167
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.Pro17Leu
CA379966490
NM_000378.6:c.50C>T