Canonical Allele Identifier: PA357877
Gene: SH3TC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 218918
ClinVar RCV Id: RCV000203275 RCV001045169
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_078853.2:p.Met1Val