Canonical Allele Identifier: PA2826136722
Gene: GRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 265191
ClinVar RCV Id: RCV000255801 RCV000678296 RCV000767020 RCV003920025
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171545.1:p.Ile534Leu
CA6674307
NM_001178074.2:c.1600A>C
CA385620513
NM_001178074.2:c.1600A>T