Canonical Allele Identifier: PA2573284442
Gene: SH3TC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1478832
ClinVar RCV Id: RCV001974374
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_078853.2:p.Leu994Pro
CA361665192
NM_024577.4:c.2981T>C