Canonical Allele Identifier: PA2825826859
Gene: LITAF HGNC NCBI

Linked Data

ClinVar Variation Id: 2703497
ClinVar RCV Id: RCV003505808

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129945.1:p.Trp116Cys
CA394765229
NM_001136473.1:c.348G>C
CA394765231
NM_001136473.1:c.348G>T