Canonical Allele Identifier: PA185793
Gene: MYL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 132976
ClinVar RCV Id: RCV000119380 RCV000156897 RCV000627045 RCV000226326
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000423.2:p.Gly162Arg
CA010431
NM_000432.4:c.484G>A
CA386696716
NM_000432.4:c.484G>C