Canonical Allele Identifier: PA2825160394
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2947909
ClinVar RCV Id: RCV003806731

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.Pro17Ser
CA379966493
NM_000378.6:c.49C>T