Canonical Allele Identifier: PA658811794
Gene: SH3TC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 543329
ClinVar RCV Id: RCV000654066 RCV002343380 RCV004533427 RCV003480743
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_078853.2:p.Arg1215His
CA3498662
NM_024577.4:c.3644G>A