Allele Registry

Canonical Allele Identifier: PA103760

Gene: SARDH HGNC NCBI

ClinVar RCV:

RCV000032643

ClinVar Variation:

39448

HGVS (amino-acid)	Matching Registered Transcripts
NP_001128179.1:p.Val71Phe	CA130303 NM_001134707.2:c.211G>T