Canonical Allele Identifier: PA2827104766
Gene: MYLK HGNC NCBI

Linked Data

ClinVar Variation Id: 1741520
ClinVar RCV Id: RCV002340228 RCV003526138
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001308238.1:p.Gln1347Arg
CA354227055
NM_001321309.2:c.4040A>G