Canonical Allele Identifier: PA100834
Gene: GP9 HGNC NCBI

Linked Data

ClinVar Variation Id: 13529
ClinVar RCV Id: RCV000014484 RCV000275909 RCV000761618 RCV001062554 RCV000851932 RCV003914843
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000165.1:p.Asn61Ser
CA123173
NM_000174.5:c.182A>G