Canonical Allele Identifier: PA2825055028
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 974171
ClinVar RCV Id: RCV001256420

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000126.2:p.Ala1399Pro
CA286614345
NM_000135.4:c.4195G>C