Canonical Allele Identifier: PA2825055007
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 855510
ClinVar RCV Id: RCV001060791

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000126.2:p.Glu1385Asp
CA397484276
NM_000135.4:c.4155G>T
CA397484277
NM_000135.4:c.4155G>C