Canonical Allele Identifier: PA2573071710
Gene: GFAP HGNC NCBI

Linked Data

ClinVar Variation Id: 1305148
ClinVar RCV Id: RCV001773858

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350775.1:p.Asn447Ser
CA399838949
NM_001363846.2:c.1340A>G