Canonical Allele Identifier: PA102529
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_002046.1:p.Asn77Ser
CA217162
NM_002055.5:c.230A>G