Canonical Allele Identifier: PA2830143028
Gene: MYLK HGNC NCBI
ClinVar RCV:
RCV002313441
ClinVar Variation:
519999
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_444260.1:p.Val139Met
CA354228503
NM_053032.4:c.415G>A