Canonical Allele Identifier: PA1139755454
Gene: SH3TC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 946186
ClinVar RCV Id: RCV001216996

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_078853.2:p.Ile1137Val
CA128997580
NM_024577.4:c.3409A>G