Canonical Allele Identifier: PA658800185
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 526402
ClinVar RCV Id: RCV000630927 RCV001120168 RCV001771851 RCV003945583
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000126.2:p.Ala635Val
CA8251971
NM_000135.4:c.1904C>T