Canonical Allele Identifier: PA237395
Gene: MYL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 191733
ClinVar RCV Id: RCV000172052 RCV000795137 RCV000852437 RCV001191379 RCV002326947 RCV003323424 RCV003995672
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000423.2:p.Asp145Asn
CA010362
NM_000432.4:c.433G>A