Canonical Allele Identifier: PA2580498563
Gene: MYLK HGNC NCBI

Linked Data

ClinVar Variation Id: 2029504
ClinVar RCV Id: RCV002880856
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_444255.3:p.Lys1485Glu
CA82918428
NM_053027.4:c.4453A>G