Canonical Allele Identifier: PA2827104731
Gene: MYLK HGNC NCBI

Linked Data

ClinVar Variation Id: 2284114
ClinVar RCV Id: RCV004136452
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001308238.1:p.Trp1314Arg
CA354227287
NM_001321309.2:c.3940T>A
CA354227288
NM_001321309.2:c.3940T>C