Canonical Allele Identifier: PA658662838
Gene: FA2H HGNC NCBI

Linked Data

ClinVar Variation Id: 447318
ClinVar RCV Id: RCV000518709 RCV000633034 RCV001310336 RCV001848887
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077282.3:p.Val309Ile
CA8170349
NM_024306.5:c.925G>A