Canonical Allele Identifier: PA113689
Gene: SH3TC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 21690
ClinVar RCV Id: RCV000020888 RCV000236498 RCV000654080 RCV001173151 RCV002415424 RCV001270096 RCV002490399
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_078853.2:p.Arg658Cys
CA342372
NM_024577.4:c.1972C>T