Canonical Allele Identifier: PA107457
Gene: MYL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 14064
ClinVar RCV Id: RCV000015108 RCV000148714 RCV000584799 RCV000620870 RCV000626337 RCV000766474 RCV001184984
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000423.2:p.Ala13Thr
CA010242
NM_000432.4:c.37G>A