Canonical Allele Identifier: PA1139671118
Gene: GP9 HGNC NCBI

Linked Data

ClinVar Variation Id: 902702

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000165.1:p.Thr44Met
CA2602638
NM_000174.5:c.131C>T