Canonical Allele Identifier: PA2580498156
Gene: MYLK HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_444253.3:p.Glu1911Val
CA82937498
NM_053025.4:c.5732A>T