Allele Registry

Canonical Allele Identifier: PA2830115611

Gene: PLAT HGNC NCBI

ClinVar RCV:

RCV001027419

ClinVar Variation:

827598

HGVS (amino-acid)	Matching Registered Transcripts
NP_127509.1:p.Trp395_Thr396delinsCysMet	CA915945660 NM_033011.4:c.1185_1187delinsTAT