Canonical Allele Identifier: PA1139690627
Gene: MYL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 854824
ClinVar RCV Id: RCV001059953 RCV002445313
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000423.2:p.Ala102Val
CA386698053
NM_000432.4:c.305C>T