Canonical Allele Identifier: PA2825083485
Gene: GP9 HGNC NCBI

Linked Data

ClinVar Variation Id: 3101078
ClinVar RCV Id: RCV004387936

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000165.1:p.Arg52Cys
CA2602646
NM_000174.5:c.154C>T