Canonical Allele Identifier: PA645414189
Gene: SH3TC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 245683
ClinVar RCV Id: RCV000235963 RCV001079256 RCV002338767 RCV004541466
ClinVar Variation Id: 476882
ClinVar RCV Id: RCV000529572 RCV000857155
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_078853.2:p.Phe399Leu
CA3499236
NM_024577.4:c.1195T>C
CA361669576
NM_024577.4:c.1197C>G
CA361669577
NM_024577.4:c.1197C>A
CA658657555
NM_024577.4:c.1194_1195delinsCC