Allele Registry

Canonical Allele Identifier: PA2827103169

Gene: MYLK HGNC NCBI

ClinVar RCV:

RCV000173911

RCV000680576

RCV000757536

RCV000769342

RCV001082109

RCV003165127

RCV003396931

ClinVar Variation:

193752

2447218

HGVS (amino-acid)	Matching Registered Transcripts
NP_001308238.1:p.Pro160Leu	CA024817 NM_001321309.2:c.479C>T CA2580068662 NM_001321309.2:c.477_479delinsTCT