Canonical Allele Identifier: PA2830137951
Gene: MYLK HGNC NCBI

Linked Data

ClinVar Variation Id: 426226

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_444254.3:p.Ala50Val
CA067424
NM_053026.4:c.149C>T