Canonical Allele Identifier: PA645375620
Gene: FA2H HGNC NCBI

Linked Data

ClinVar Variation Id: 381515
ClinVar RCV Id: RCV000633072 RCV001712218 RCV001115914 RCV001848762 RCV001821170 RCV002524896
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077282.3:p.Arg113Trp
CA8170582
NM_024306.5:c.337C>T