Canonical Allele Identifier: PA100879
Gene: GP9 HGNC NCBI

Linked Data

ClinVar Variation Id: 13534
ClinVar RCV Id: RCV000014489 RCV003556014
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000165.1:p.Leu7Pro
CA123183
NM_000174.5:c.20T>C