Canonical Allele Identifier: PA159336
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 134277

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000126.2:p.Ser103Leu
CA159334
NM_000135.4:c.308C>T