Allele Registry

Canonical Allele Identifier: PA915965803

Gene: PLAT HGNC NCBI

ClinVar RCV:

RCV001027419

ClinVar Variation:

827598

HGVS (amino-acid)	Matching Registered Transcripts
NP_000921.1:p.Trp441_Thr442delinsCysMet	CA915945660 NM_000930.5:c.1323_1325delinsTAT