Allele Registry

Canonical Allele Identifier: PA2827034261

Gene: PLAT HGNC NCBI

ClinVar RCV:

RCV001027419

ClinVar Variation:

827598

HGVS (amino-acid)	Matching Registered Transcripts
NP_001306118.1:p.Trp352_Thr353delinsCysMet	CA915945660 NM_001319189.2:c.1056_1058delinsTAT