Allele Registry

Canonical Allele Identifier: PA100874

Gene: GP9 HGNC NCBI

ClinVar RCV:

RCV000014487

ClinVar Variation:

13532

HGVS (amino-acid)	Matching Registered Transcripts
NP_000165.1:p.Leu56Pro	CA123179 NM_000174.5:c.167T>C