Canonical Allele Identifier: PA645414248
Gene: SH3TC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 377021
ClinVar RCV Id: RCV000441336 RCV000456313 RCV000789561 RCV001353153
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_078853.2:p.Asn881Ser
CA3498953
NM_024577.4:c.2642A>G