Canonical Allele Identifier: PA916031225
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 134277

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338759.1:p.Ser103Leu
CA159334
NM_001351830.2:c.308C>T