Canonical Allele Identifier: PA645477210
Gene: TSPAN12 HGNC NCBI

Linked Data

ClinVar Variation Id: 236067
ClinVar RCV Id: RCV000225062 RCV000225079 RCV000225020 RCV001003234 RCV003328570
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_036470.1:p.Cys181Phe
CA10581517
NM_012338.4:c.542G>T