Canonical Allele Identifier: PA645404152
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 321351

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000126.2:p.Met664Val
CA8251962
NM_000135.4:c.1990A>G