Canonical Allele Identifier: PA2742001597
Gene: MYLK HGNC NCBI

Linked Data

ClinVar Variation Id: 2577622
ClinVar RCV Id: RCV003324959
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_444255.3:p.Leu1538Met
CA354226952
NM_053027.4:c.4612C>A