Allele Registry

Canonical Allele Identifier: PA296982

Gene: MYL3 HGNC NCBI

ClinVar RCV:

RCV000158941

RCV002415694

ClinVar Variation:

181440

HGVS (amino-acid)	Matching Registered Transcripts
NP_000249.1:p.Pro65Arg	CA013649 NM_000258.3:c.194C>G