Canonical Allele Identifier: PA2830139534
Gene: MYLK HGNC NCBI

Linked Data

ClinVar Variation Id: 2912060

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_444254.3:p.Ser1430Thr
CA354227224
NM_053026.4:c.4288T>A