Canonical Allele Identifier: PA2830434169
Gene: MLX HGNC NCBI

Linked Data

ClinVar Variation Id: 3211029
ClinVar RCV Id: RCV004505417
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937847.1:p.Val232Ala
CA399605174
NM_198204.2:c.695T>C