Canonical Allele Identifier: PA645414175
Gene: SH3TC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 407269
ClinVar RCV Id: RCV000457307 RCV000765821 RCV000992973 RCV002339147 RCV001174034
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_078853.2:p.Leu173Met
CA3499489
NM_024577.4:c.517C>A