Canonical Allele Identifier: PA2829976728
Gene: GRIN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2413080
ClinVar RCV Id: RCV003110095
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_067544.1:p.Thr335Ser
CA375715363
NM_021569.4:c.1003A>T
CA375715365
NM_021569.4:c.1004C>G