Canonical Allele Identifier: PA2830139866
Gene: MYLK HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_444254.3:p.Asp1808Tyr
CA354228835
NM_053026.4:c.5422G>T