Allele Registry

Canonical Allele Identifier: PA658662827

Gene: FA2H HGNC NCBI

ClinVar RCV:

RCV000555976

RCV002265790

ClinVar Variation:

458305

HGVS (amino-acid)	Matching Registered Transcripts
NP_077282.3:p.Pro44Gln	CA283770000 NM_024306.5:c.131C>A