Canonical Allele Identifier: PA2828120181
Gene: GFAP HGNC NCBI

Linked Data

ClinVar Variation Id: 66468
ClinVar RCV Id: RCV000056865 RCV000192107
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350775.1:p.Asn77Ser
CA217162
NM_001363846.2:c.230A>G