Canonical Allele Identifier: PA2828218691
Gene: GRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 227419
ClinVar RCV Id: RCV000216399 RCV000726538 RCV001114156 RCV001252265
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001353653.1:p.Met768Arg
CA6674142
NM_001366724.1:c.2303T>G