Canonical Allele Identifier: PA916014866
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 237034

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273096.1:p.Ser447Leu
CA8252400
NM_001286167.3:c.1340C>T