Canonical Allele Identifier: PA092270
Gene: TSPAN12 HGNC NCBI

Linked Data

ClinVar Variation Id: 126503
ClinVar RCV Id: RCV000114398

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_036470.1:p.Tyr138Cys
CA269452
NM_012338.4:c.413A>G