Canonical Allele Identifier: PA2580462789
Gene: SH3TC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1909339
ClinVar RCV Id: RCV002587356
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_078853.2:p.Ala989Thr
CA361665229
NM_024577.4:c.2965G>A