Allele Registry

Canonical Allele Identifier: PA2830140298

Gene: MYLK HGNC NCBI

ClinVar RCV:

RCV000173911

RCV000680576

RCV000757536

RCV000769342

RCV001082109

RCV003165127

RCV003396931

ClinVar Variation:

193752

2447218

HGVS (amino-acid)	Matching Registered Transcripts
NP_444255.3:p.Pro336Leu	CA024817 NM_053027.4:c.1007C>T CA2580068662 NM_053027.4:c.1005_1007delinsTCT