Canonical Allele Identifier: PA183365
Gene: MYL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 178948
ClinVar RCV Id: RCV000155724 RCV000530339 RCV000852438 RCV001555854
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000423.2:p.Ala141Thr
CA010334
NM_000432.4:c.421G>A