Allele Registry

Canonical Allele Identifier: PA113236

Gene: FA2H HGNC NCBI

ClinVar RCV:

RCV000001099

ClinVar Variation:

1044

HGVS (amino-acid)	Matching Registered Transcripts
NP_077282.3:p.Asp35Tyr	CA251671 NM_024306.5:c.103G>T