Canonical Allele Identifier: PA113695
Gene: SH3TC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 21689
ClinVar RCV Id: RCV000020887 RCV000206757 RCV000857147 RCV002496432
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_078853.2:p.Glu657Lys
CA339774
NM_024577.4:c.1969G>A