Canonical Allele Identifier: PA2742001596
Gene: MYLK HGNC NCBI

Linked Data

ClinVar Variation Id: 2838241
ClinVar RCV Id: RCV003641785

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_444255.3:p.Met1536Thr
CA354226964
NM_053027.4:c.4607T>C