Canonical Allele Identifier: PA2573284444
Gene: SH3TC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1375186

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_078853.2:p.Glu1000Ala
CA3498880
NM_024577.4:c.2999A>C