Allele Registry

Canonical Allele Identifier: PA2827103697

Gene: MYLK HGNC NCBI

ClinVar RCV:

RCV000648721

RCV000735407

RCV000762384

RCV002313418

RCV002491329

ClinVar Variation:

519975

HGVS (amino-acid)	Matching Registered Transcripts
NP_001308238.1:p.Asp541Asn	CA068219 NM_001321309.2:c.1621G>A