Canonical Allele Identifier: PA2830141556
Gene: MYLK HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_444255.3:p.Glu1860Val
CA82937498
NM_053027.4:c.5579A>T