Allele Registry

Canonical Allele Identifier: PA296996

Gene: MYL3 HGNC NCBI

ClinVar RCV:

RCV000158960

RCV003532002

ClinVar Variation:

181447

HGVS (amino-acid)	Matching Registered Transcripts
NP_000249.1:p.Pro65Ser	CA013638 NM_000258.3:c.193C>T