Canonical Allele Identifier: PA658810664
Gene: FA2H HGNC NCBI

Linked Data

ClinVar Variation Id: 528011
ClinVar RCV Id: RCV000633060
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077282.3:p.Thr352Ile
CA396768762
NM_024306.5:c.1055C>T