Canonical Allele Identifier: PA113701
Gene: SH3TC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2485
ClinVar RCV Id: RCV000002591 RCV000002590 RCV000415264 RCV000656975 RCV001079620 RCV001172848 RCV001293355 RCV001705579 RCV002345223
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_078853.2:p.Tyr169His
CA115576
NM_024577.4:c.505T>C