Canonical Allele Identifier: PA913198353
Gene: FA2H HGNC NCBI

Linked Data

ClinVar Variation Id: 623362
ClinVar RCV Id: RCV000761510
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077282.3:p.His69Gln
CA283769920
NM_024306.5:c.207C>G
CA396768192
NM_024306.5:c.207C>A