Allele Registry

Canonical Allele Identifier: PA110378

Gene: SAMD9 HGNC NCBI

ClinVar RCV:

RCV000001288

RCV003555884

ClinVar Variation:

1229

HGVS (amino-acid)	Matching Registered Transcripts
NP_001180236.1:p.Lys1495Glu	CA114859 NM_001193307.1:c.4483A>G