Canonical Allele Identifier: PA2827104777
Gene: MYLK HGNC NCBI

Linked Data

ClinVar Variation Id: 1317223

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001308238.1:p.Lys1355Asn
CA071839
NM_001321309.2:c.4065G>C
CA354226994
NM_001321309.2:c.4065G>T