Canonical Allele Identifier: PA916052333
Gene: MYLK HGNC NCBI

Linked Data

ClinVar Variation Id: 426226
ClinVar RCV Id: RCV000489357 RCV001851307 RCV000769346
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_444256.3:p.Ala50Val
CA067424
NM_053028.4:c.149C>T