Canonical Allele Identifier: PA2826136650
Gene: GRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 493119
ClinVar RCV Id: RCV000585386 RCV002506395
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171545.1:p.Arg339Trp
CA6674480
NM_001178074.2:c.1015C>T