Canonical Allele Identifier: PA2828218251
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_001353652.1:p.Ile522Val
CA6674335
NM_001366723.1:c.1564A>G