Canonical Allele Identifier: PA104122
Gene: LITAF HGNC NCBI

Linked Data

ClinVar Variation Id: 215840

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129944.1:p.Thr49Met
CA338014
NM_001136472.2:c.146C>T