Canonical Allele Identifier: PA915982278
Gene: LITAF HGNC NCBI

Linked Data

ClinVar Variation Id: 654391
ClinVar RCV Id: RCV000810352
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004853.2:p.Val79Ala
CA394766064
NM_004862.4:c.236T>C