Allele Registry

Canonical Allele Identifier: PA113220

Gene: FA2H HGNC NCBI

ClinVar Allele:

39829

ClinVar RCV:

RCV000023857

RCV000483483

RCV002513207

RCV003317044

ClinVar Variation:

30872

HGVS (amino-acid)	Matching Registered Transcripts
NP_077282.3:p.Arg154Cys	CA259930 NM_024306.5:c.460C>T