Canonical Allele Identifier: PA2827105102
Gene: MYLK HGNC NCBI

Linked Data

ClinVar Variation Id: 222741
ClinVar RCV Id: RCV000208152 RCV002265686 RCV002503823 RCV002517400
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001308238.1:p.Arg1640His
CA072986
NM_001321309.2:c.4919G>A