Allele Registry

Canonical Allele Identifier: PA342376

Gene: SH3TC2 HGNC NCBI

ClinVar RCV:

RCV000790207

ClinVar Variation:

21691

HGVS (amino-acid)	Matching Registered Transcripts
NP_078853.2:p.Leu661Pro	CA342374 NM_024577.4:c.1982T>C