Canonical Allele Identifier: PA658802989
Gene: MYL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 532776
ClinVar RCV Id: RCV000639675 RCV002223234
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000423.2:p.Pro143Thr
CA386696952
NM_000432.4:c.427C>A