Allele Registry

Canonical Allele Identifier: PA130304

Gene: SARDH HGNC NCBI

ClinVar RCV:

RCV000032643

ClinVar Variation:

39448

HGVS (amino-acid)	Matching Registered Transcripts
NP_009032.2:p.Val71Phe	CA130303 NM_007101.3:c.211G>T