Canonical Allele Identifier: PA2830139564
Gene: MYLK HGNC NCBI

Linked Data

ClinVar Variation Id: 1317223

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_444254.3:p.Lys1462Asn
CA071839
NM_053026.4:c.4386G>C
CA354226994
NM_053026.4:c.4386G>T