Canonical Allele Identifier: PA891849209
Gene: MYL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 571147
ClinVar RCV Id: RCV000692199 RCV001538762 RCV002424631
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000423.2:p.Gly87Glu
CA386698668
NM_000432.4:c.260G>A