Canonical Allele Identifier: PA891865436
Gene: GFAP HGNC NCBI

Linked Data

ClinVar Variation Id: 590968
ClinVar RCV Id: RCV000722139

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002046.1:p.Asn375Lys
CA399843303
NM_002055.5:c.1125C>G
CA399843304
NM_002055.5:c.1125C>A