Allele Registry

Canonical Allele Identifier: PA342382

Gene: SH3TC2 HGNC NCBI

ClinVar RCV:

RCV000789693

ClinVar Variation:

21695

HGVS (amino-acid)	Matching Registered Transcripts
NP_078853.2:p.Asn881Ile	CA342380 NM_024577.4:c.2642A>T