Canonical Allele Identifier: PA2829873001
Gene: FANCL HGNC NCBI

Linked Data

ClinVar Variation Id: 1378618
ClinVar RCV Id: RCV001890201
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060532.2:p.Pro360Ala
CA1670316
NM_018062.4:c.1078C>G