Allele Registry

Canonical Allele Identifier: PA260037

Gene: FA2H HGNC NCBI

ClinVar Allele:

40302

ClinVar RCV:

RCV000024321

ClinVar Variation:

31624

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