Canonical Allele Identifier: PA2830141541
Gene: MYLK HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_444255.3:p.Val1848Met
CA354228503
NM_053027.4:c.5542G>A