Allele Registry

Canonical Allele Identifier: PA130306

Gene: SARDH HGNC NCBI

ClinVar RCV:

RCV000032644

ClinVar Variation:

39449

HGVS (amino-acid)	Matching Registered Transcripts
NP_009032.2:p.Pro287Leu	CA130305 NM_007101.3:c.860C>T