Canonical Allele Identifier: PA2830142632
Gene: MYLK HGNC NCBI

Linked Data

ClinVar Variation Id: 1741520

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_444256.3:p.Gln1454Arg
CA354227055
NM_053028.4:c.4361A>G