Allele Registry

Canonical Allele Identifier: PA916052017

Gene: MYLK HGNC NCBI

ClinVar RCV:

RCV000198643

RCV002315630

ClinVar Variation:

216969

HGVS (amino-acid)	Matching Registered Transcripts
NP_444255.3:p.Asp717Tyr	CA068222 NM_053027.4:c.2149G>T