Canonical Allele Identifier: PA1139671124
Gene: GP9 HGNC NCBI

Linked Data

ClinVar Variation Id: 902703
ClinVar RCV Id: RCV001149441

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000165.1:p.Pro68Leu
CA2602662
NM_000174.5:c.203C>T