Allele Registry

Canonical Allele Identifier: PA159541

Gene: FANCE HGNC NCBI

ClinVar Allele:

138077

ClinVar RCV:

RCV000121012

RCV001153476

ClinVar Variation:

134338

HGVS (amino-acid)	Matching Registered Transcripts
NP_068741.1:p.Arg365Ser	CA159539 NM_021922.3:c.1095A>C CA363775457 NM_021922.3:c.1095A>T