Canonical Allele Identifier: PA658811763
Gene: SH3TC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 543306
ClinVar RCV Id: RCV000654040

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_078853.2:p.Asn1013Lys
CA3498870
NM_024577.4:c.3039C>A
CA361665073
NM_024577.4:c.3039C>G