Canonical Allele Identifier: PA356154
Gene: FANCL HGNC NCBI

Linked Data

ClinVar Variation Id: 221092
ClinVar RCV Id: RCV000420428 RCV000515051 RCV001137465 RCV001082870 RCV003937791
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060532.2:p.Leu38Phe
CA350328
NM_018062.4:c.112C>T
CA645534776
NM_018062.4:c.111_112delinsTT