Canonical Allele Identifier: PA2827104770
Gene: MYLK HGNC NCBI

Linked Data

ClinVar Variation Id: 2920836
ClinVar RCV Id: RCV003736403

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001308238.1:p.Val1349Met
CA354227043
NM_001321309.2:c.4045G>A