Canonical Allele Identifier: PA915982755
Gene: LRTOMT HGNC NCBI

Linked Data

ClinVar Variation Id: 163941
ClinVar RCV Id: RCV000150998
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001138781.1:p.His55Gln
CA176672
NM_001145309.4:c.165C>G
CA381717244
NM_001145309.4:c.165C>A