Canonical Allele Identifier: PA2830139571
Gene: MYLK HGNC NCBI

Linked Data

ClinVar Variation Id: 2838241
ClinVar RCV Id: RCV003641785

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_444254.3:p.Met1467Thr
CA354226964
NM_053026.4:c.4400T>C