Allele Registry

Canonical Allele Identifier: PA2580552915

Gene: SNX20 HGNC NCBI

ClinVar RCV:

RCV004110390

ClinVar Variation:

2254648

HGVS (amino-acid)	Matching Registered Transcripts
NP_878274.1:p.Asp271Val	CA395870804 NM_182854.4:c.812A>T