Canonical Allele Identifier: PA2825826788
Gene: LITAF HGNC NCBI

Linked Data

ClinVar Variation Id: 654391
ClinVar RCV Id: RCV000810352

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129945.1:p.Val79Ala
CA394766064
NM_001136473.1:c.236T>C