Canonical Allele Identifier: PA2825055003
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 2084285
ClinVar RCV Id: RCV003011061

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000126.2:p.Ser1383Arg
CA397484289
NM_000135.4:c.4149C>G
CA397484290
NM_000135.4:c.4149C>A
CA397484295
NM_000135.4:c.4147A>C