Canonical Allele Identifier: PA133448
Gene: LRTOMT HGNC NCBI

Linked Data

ClinVar Variation Id: 44041
ClinVar RCV Id: RCV000037016
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001138780.1:p.Asp224Glu
CA133447
NM_001145308.4:c.672C>G
CA381724662
NM_001145308.4:c.672C>A