Canonical Allele Identifier: PA2580498566
Gene: MYLK HGNC NCBI

Linked Data

ClinVar Variation Id: 2284114
ClinVar RCV Id: RCV004136452

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_444255.3:p.Trp1490Arg
CA354227287
NM_053027.4:c.4468T>A
CA354227288
NM_053027.4:c.4468T>C