Canonical Allele Identifier: PA2830142974
Gene: MYLK HGNC NCBI
ClinVar RCV:
RCV002347735
ClinVar Variation:
1749335
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_444259.1:p.Glu150Val
CA82937498
NM_053031.4:c.449A>T