Canonical Allele Identifier: PA658654587
Gene: MYH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 445951
ClinVar RCV Id: RCV000513939 RCV000764101
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060004.3:p.Ala1708Thr
CA8390487
NM_017534.6:c.5122G>A