Canonical Allele Identifier: PA2825329013
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 134277

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001018122.1:p.Ser103Leu
CA159334
NM_001018112.2:c.308C>T