Allele Registry

Canonical Allele Identifier: PA103749

Gene: SARDH HGNC NCBI

ClinVar RCV:

RCV000032644

ClinVar Variation:

39449

HGVS (amino-acid)	Matching Registered Transcripts
NP_001128179.1:p.Pro287Leu	CA130305 NM_001134707.2:c.860C>T