Allele Registry

Canonical Allele Identifier: PA296970

Gene: MYL2 HGNC NCBI

ClinVar RCV:

RCV000158925

RCV001180080

RCV001370474

RCV002247553

RCV002426780

RCV003998374

ClinVar Variation:

181432

HGVS (amino-acid)	Matching Registered Transcripts
NP_000423.2:p.Phe86Ser	CA009962 NM_000432.4:c.257T>C