Canonical Allele Identifier: PA2830139525
Gene: MYLK HGNC NCBI

Linked Data

ClinVar Variation Id: 2284114
ClinVar RCV Id: RCV004136452

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_444254.3:p.Trp1421Arg
CA354227287
NM_053026.4:c.4261T>A
CA354227288
NM_053026.4:c.4261T>C