Allele Registry

Canonical Allele Identifier: PA2573169300

Gene: MYL2 HGNC NCBI

ClinVar RCV:

RCV001887426

ClinVar Variation:

1396446

HGVS (amino-acid)	Matching Registered Transcripts
NP_000423.2:p.Pro95Ser	CA386698143 NM_000432.4:c.283C>T