Canonical Allele Identifier: PA2828218206
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_001353652.1:p.Ser406Ile
CA16609528
NM_001366723.1:c.1217G>T