Canonical Allele Identifier: PA2830142805
Gene: MYLK HGNC NCBI

Linked Data

ClinVar Variation Id: 252775

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_444256.3:p.Ala1706Val
CA073013
NM_053028.4:c.5117C>T