Canonical Allele Identifier: PA658660002
Gene: SH3TC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 451327
ClinVar RCV Id: RCV000520904 RCV000536439 RCV001173166 RCV002323889
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_078853.2:p.Ala1043Ser
CA3498845
NM_024577.4:c.3127G>T