Allele Registry

Canonical Allele Identifier: PA2580387008

Gene: WSCD1 HGNC NCBI

ClinVar RCV:

RCV004091344

ClinVar Variation:

2227707

HGVS (amino-acid)	Matching Registered Transcripts
NP_056068.1:p.Ser469Leu	CA8328152 NM_015253.2:c.1406C>T