Canonical Allele Identifier: PA2830142636
Gene: MYLK HGNC NCBI

Linked Data

ClinVar Variation Id: 2920836
ClinVar RCV Id: RCV003736403

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_444256.3:p.Val1456Met
CA354227043
NM_053028.4:c.4366G>A