Canonical Allele Identifier: PA2573284454
Gene: SH3TC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1482002

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_078853.2:p.Arg1012Gln
CA3498871
NM_024577.4:c.3035G>A