Allele Registry

Canonical Allele Identifier: PA093253

Gene: SOST HGNC NCBI

ClinVar RCV:

RCV000024298

ClinVar Variation:

31593

HGVS (amino-acid)	Matching Registered Transcripts
NP_079513.1:p.Val21Leu	CA399703409 NM_025237.3:c.61G>T CA399703411 NM_025237.3:c.61G>C