Canonical Allele Identifier: PA645414285
Gene: SH3TC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 351901
ClinVar RCV Id: RCV000327954 RCV000654217 RCV000857794 RCV002446605
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_078853.2:p.Ala1017Thr
CA3498867
NM_024577.4:c.3049G>A