Canonical Allele Identifier: PA2742001480
Gene: MYLK HGNC NCBI

Linked Data

ClinVar Variation Id: 2805359
ClinVar RCV Id: RCV003641391

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_444255.3:p.Ile744Met
CA354233992
NM_053027.4:c.2232A>G