Canonical Allele Identifier: PA2580193566
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 2084285
ClinVar RCV Id: RCV003011061

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273096.1:p.Ser1383Arg
CA397484289
NM_001286167.3:c.4149C>G
CA397484290
NM_001286167.3:c.4149C>A
CA397484295
NM_001286167.3:c.4147A>C