Canonical Allele Identifier: PA2826136713
Gene: GRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 381678
ClinVar RCV Id: RCV000434726 RCV001110879 RCV003922752
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171545.1:p.Ile497Val
CA6674335
NM_001178074.2:c.1489A>G