Canonical Allele Identifier: PA916015114
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 134269
ClinVar RCV Id: RCV000120942 RCV000204450 RCV001115378 RCV003407512 RCV003952597
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273096.1:p.Arg1195Trp
CA332149
NM_001286167.3:c.3583C>T