Canonical Allele Identifier: PA104098
Gene: LITAF HGNC NCBI

Linked Data

ClinVar Variation Id: 6057

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129944.1:p.Gly112Ser
CA340507
NM_001136472.2:c.334G>A