Canonical Allele Identifier: PA110836
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 430085
ClinVar RCV Id: RCV000494388 RCV000666624 RCV001219227
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000126.2:p.Pro1324Leu
CA8250847
NM_000135.4:c.3971C>T
CA2695223848
NM_000135.4:c.3971_3972delinsTT