Canonical Allele Identifier: PA2830138688
Gene: MYLK HGNC NCBI

Linked Data

ClinVar Variation Id: 2805359
ClinVar RCV Id: RCV003641391

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_444254.3:p.Ile675Met
CA354233992
NM_053026.4:c.2025A>G