Canonical Allele Identifier: PA2827104715
Gene: MYLK HGNC NCBI

Linked Data

ClinVar Variation Id: 1015193
ClinVar RCV Id: RCV001314019 RCV002329264 RCV002504481
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001308238.1:p.Arg1304Gln
CA354227347
NM_001321309.2:c.3911G>A