Canonical Allele Identifier: PA645375754
Gene: FA2H HGNC NCBI

Linked Data

ClinVar Variation Id: 320495
ClinVar RCV Id: RCV000383560 RCV000416009 RCV001080196 RCV001848663 RCV002307485
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077282.3:p.Gly282Ser
CA8170371
NM_024306.5:c.844G>A