Canonical Allele Identifier: PA2827105207
Gene: MYLK HGNC NCBI
ClinVar RCV:
RCV002347735
ClinVar Variation:
1749335
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001308238.1:p.Glu1735Val
CA82937498
NM_001321309.2:c.5204A>T