Allele Registry

Canonical Allele Identifier: PA1139690638

Gene: MYL2 HGNC NCBI

ClinVar RCV:

RCV001114909

ClinVar Variation:

884051

HGVS (amino-acid)	Matching Registered Transcripts
NP_000423.2:p.Arg120Leu	CA386697804 NM_000432.4:c.359G>T