Canonical Allele Identifier: PA891847873
Gene: LITAF HGNC NCBI

Linked Data

ClinVar Variation Id: 581607
ClinVar RCV Id: RCV000705486
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004853.2:p.Pro91Leu
CA394765763
NM_004862.4:c.272C>T