Canonical Allele Identifier: PA645404527
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 321335
ClinVar RCV Id: RCV000287104 RCV000484383 RCV001094249 RCV003912330
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000126.2:p.Arg1184Pro
CA8251098
NM_000135.4:c.3551G>C