Canonical Allele Identifier: PA658659944
Gene: SH3TC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 476881
ClinVar RCV Id: RCV000555948 RCV002330973 RCV003226947 RCV004543243
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_078853.2:p.Ala393Val
CA3499240
NM_024577.4:c.1178C>T