Allele Registry

Canonical Allele Identifier: PA645493578

Gene: NSMCE3 HGNC NCBI

ClinVar RCV:

RCV000258643

RCV000412556

ClinVar Variation:

267796

HGVS (amino-acid)	Matching Registered Transcripts
NP_619649.1:p.Pro209Leu	CA10602639 NM_138704.4:c.626C>T