Canonical Allele Identifier: PA2828530059
Gene: FANCL HGNC NCBI

Linked Data

ClinVar Variation Id: 2054645
ClinVar RCV Id: RCV002909834
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361544.1:p.Met84Ile
CA347034652
NM_001374615.1:c.252G>T
CA347034653
NM_001374615.1:c.252G>C
CA347034654
NM_001374615.1:c.252G>A