Canonical Allele Identifier: PA095378
Gene: MYLK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 4244
ClinVar RCV Id: RCV000004466 RCV000154782 RCV001170850 RCV000467194 RCV001701560
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_149109.1:p.Ala95Glu
CA116736
NM_033118.4:c.284C>A