Canonical Allele Identifier: PA658661972
Gene: FANCL HGNC NCBI

Linked Data

ClinVar Variation Id: 456243
ClinVar RCV Id: RCV000552744 RCV001137464 RCV001821482 RCV003925582
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060532.2:p.Arg68Pro
CA1670757
NM_018062.4:c.203G>C