Allele Registry

Canonical Allele Identifier: PA915965894

Gene: MYL2 HGNC NCBI

ClinVar RCV:

RCV000988908

ClinVar Variation:

802892

HGVS (amino-acid)	Matching Registered Transcripts
NP_000423.2:p.Ala55Pro	CA386699176 NM_000432.4:c.163G>C