Allele Registry

Canonical Allele Identifier: PA2829178705

Gene: WSCD1 HGNC NCBI

ClinVar RCV:

RCV004091344

ClinVar Variation:

2227707

HGVS (amino-acid)	Matching Registered Transcripts
NP_001375338.1:p.Ser301Leu	CA8328152 NM_001388409.1:c.902C>T