Canonical Allele Identifier: PA260037
Gene: FA2H HGNC NCBI

Linked Data

ClinVar Variation Id: 31624
ClinVar RCV Id: RCV000024321
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077282.3:p.Phe236Ser
CA260036
NM_024306.5:c.707T>C