Allele Registry

Canonical Allele Identifier: PA113695

Gene: SH3TC2 HGNC NCBI

ClinVar RCV:

RCV000020887

RCV000206757

RCV000857147

RCV002496432

ClinVar Variation:

21689

HGVS (amino-acid)	Matching Registered Transcripts
NP_078853.2:p.Glu657Lys	CA339774 NM_024577.4:c.1969G>A