Canonical Allele Identifier: PA2573225875
Gene: MYL4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1378952
ClinVar RCV Id: RCV001883525
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002467.1:p.Leu111Pro
CA400022197
NM_002476.2:c.332T>C