Canonical Allele Identifier: PA891853060
Gene: SH3TC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 575988
ClinVar RCV Id: RCV000698355
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_078853.2:p.Ala979Ser
CA128983454
NM_024577.4:c.2935G>T