Allele Registry

Canonical Allele Identifier: PA916052018

Gene: MYLK HGNC NCBI

ClinVar RCV:

RCV000648721

RCV000735407

RCV000762384

RCV002313418

RCV002491329

ClinVar Variation:

519975

HGVS (amino-acid)	Matching Registered Transcripts
NP_444255.3:p.Asp717Asn	CA068219 NM_053027.4:c.2149G>A