Canonical Allele Identifier: PA915982793
Gene: LRTOMT HGNC NCBI

Linked Data

ClinVar Variation Id: 44041
ClinVar RCV Id: RCV000037016

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001138781.1:p.Asp224Glu
CA133447
NM_001145309.4:c.672C>G
CA381724662
NM_001145309.4:c.672C>A