Canonical Allele Identifier: PA2830139538
Gene: MYLK HGNC NCBI

Linked Data

ClinVar Variation Id: 264262
ClinVar RCV Id: RCV002311117
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_444254.3:p.Arg1438Gln
CA10587551
NM_053026.4:c.4313G>A