Canonical Allele Identifier: PA259929
Gene: FA2H HGNC NCBI

Linked Data

ClinVar Variation Id: 30871
ClinVar RCV Id: RCV000023856 RCV002293414 RCV002513206
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077282.3:p.Arg53_Ile58del
CA259928
NM_024306.5:c.159_176del