Canonical Allele Identifier: PA1139720150
Gene: TSPAN12 HGNC NCBI

Linked Data

ClinVar Variation Id: 958329
ClinVar RCV Id: RCV001231477

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_036470.1:p.Asn137Asp
CA165837052
NM_012338.4:c.409A>G