Canonical Allele Identifier: PA915982280
Gene: LITAF HGNC NCBI

Linked Data

ClinVar Variation Id: 642426
ClinVar RCV Id: RCV000795892
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004853.2:p.Tyr80Cys
CA7904104
NM_004862.4:c.239A>G