Canonical Allele Identifier: PA645375623
Gene: FA2H HGNC NCBI

Linked Data

ClinVar Variation Id: 241461
ClinVar RCV Id: RCV000514460 RCV000419332 RCV001084384 RCV001848010 RCV001115913
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077282.3:p.Arg113Gln
CA8170581
NM_024306.5:c.338G>A