Canonical Allele Identifier: PA2830143039
Gene: MYLK HGNC NCBI
ClinVar RCV:
RCV002347735
ClinVar Variation:
1749335
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_444260.1:p.Glu151Val
CA82937498
NM_053032.4:c.452A>T