Canonical Allele Identifier: PA916052256
Gene: MYLK HGNC NCBI

Linked Data

ClinVar Variation Id: 264262
ClinVar RCV Id: RCV002311117
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_444255.3:p.Arg1507Gln
CA10587551
NM_053027.4:c.4520G>A