Canonical Allele Identifier: PA658819468
Gene: MYLK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 540257
ClinVar RCV Id: RCV000650230
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_149109.1:p.Gly23Asp
CA9802834
NM_033118.4:c.68G>A