Canonical Allele Identifier: PA2830139767
Gene: MYLK HGNC NCBI

Linked Data

ClinVar Variation Id: 30133

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_444254.3:p.Ser1690Pro
CA024862
NM_053026.4:c.5068T>C