Canonical Allele Identifier: PA645414244
Gene: SH3TC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 245730
ClinVar RCV Id: RCV000236438 RCV001037566 RCV003243030
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_078853.2:p.Arg851Trp
CA3498971
NM_024577.4:c.2551C>T