Canonical Allele Identifier: PA658811758
Gene: SH3TC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 497745

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_078853.2:p.Pro975Ala
CA361665319
NM_024577.4:c.2923C>G