Canonical Allele Identifier: PA915982790
Gene: LRTOMT HGNC NCBI

Linked Data

ClinVar Variation Id: 305997
ClinVar RCV Id: RCV000386764

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001138781.1:p.Pro198Ser
CA10640066
NM_001145309.4:c.592C>T