Allele Registry

Canonical Allele Identifier: PA2828218806

Gene: RASD2 HGNC NCBI

ClinVar RCV:

RCV004231348

ClinVar Variation:

2398612

HGVS (amino-acid)	Matching Registered Transcripts
NP_001353654.1:p.Ser161Leu	CA411348255 NM_001366725.1:c.482C>T