Canonical Allele Identifier: PA916076965
Gene: SH3TC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 637412
ClinVar RCV Id: RCV000789573 RCV001044556 RCV002458407 RCV003330952
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_078853.2:p.Arg1127Trp
CA361664656
NM_024577.4:c.3379C>T