Canonical Allele Identifier: PA2825826547
Gene: LITAF HGNC NCBI

Linked Data

ClinVar Variation Id: 41229

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129944.1:p.Ala111Gly
CA344230
NM_001136472.2:c.332C>G