Canonical Allele Identifier: PA645414185
Gene: SH3TC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 246592
ClinVar RCV Id: RCV000728925 RCV001174028 RCV001689763 RCV002460063 RCV002519835 RCV003387818 RCV004529417
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_078853.2:p.Met334Val
CA3499333
NM_024577.4:c.1000A>G