Canonical Allele Identifier: PA2829353310
Gene: GFAP HGNC NCBI

Linked Data

ClinVar Variation Id: 1305148
ClinVar RCV Id: RCV001773858
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002046.1:p.Asn407Ser
CA399838949
NM_002055.5:c.1220A>G