Allele Registry

Canonical Allele Identifier: PA2580306281

Gene: WNT11 HGNC NCBI

ClinVar RCV:

RCV004231124

ClinVar Variation:

2397360

HGVS (amino-acid)	Matching Registered Transcripts
NP_004617.2:p.Lys26Asn	CA224751214 NM_004626.3:c.78G>C CA381905095 NM_004626.3:c.78G>T