Allele Registry

Canonical Allele Identifier: PA2830138667

Gene: MYLK HGNC NCBI

ClinVar RCV:

RCV000198643

RCV002315630

ClinVar Variation:

216969

HGVS (amino-acid)	Matching Registered Transcripts
NP_444254.3:p.Asp648Tyr	CA068222 NM_053026.4:c.1942G>T