Canonical Allele Identifier: PA2826136668
Gene: GRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 402209
ClinVar RCV Id: RCV000454347
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171545.1:p.Ser381Ile
CA16609528
NM_001178074.2:c.1142G>T