Canonical Allele Identifier: PA2573062695
Gene: MYL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1335831
ClinVar RCV Id: RCV001822034 RCV001885309 RCV004040956
ClinVar Variation Id: 2046379
ClinVar RCV Id: RCV002913647
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000423.2:p.Gly87Arg
CA386698670
NM_000432.4:c.259G>C
CA386698671
NM_000432.4:c.259G>A