Allele Registry

Canonical Allele Identifier: PA2829178505

Gene: WSCD1 HGNC NCBI

ClinVar RCV:

RCV004091344

ClinVar Variation:

2227707

HGVS (amino-acid)	Matching Registered Transcripts
NP_001375334.1:p.Ser469Leu	CA8328152 NM_001388405.1:c.1406C>T