Canonical Allele Identifier: PA107488
Gene: MYL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 14065
ClinVar RCV Id: RCV000015109 RCV000158914 RCV000234985 RCV000768488 RCV001170438 RCV002354163 RCV004532354
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000423.2:p.Glu22Lys
CA010513
NM_000432.4:c.64G>A