Canonical Allele Identifier: PA2827103695
Gene: MYLK HGNC NCBI

Linked Data

ClinVar Variation Id: 216969
ClinVar RCV Id: RCV000198643 RCV002315630
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001308238.1:p.Asp541Tyr
CA068222
NM_001321309.2:c.1621G>T