Canonical Allele Identifier: PA2828965430
Gene: LOXHD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2428081
ClinVar RCV Id: RCV003117052
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001371403.1:p.Gly1561Arg
CA8952312
NM_001384474.1:c.4681G>A
CA402373239
NM_001384474.1:c.4681G>C