Canonical Allele Identifier: PA645495320
Gene: MYH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 225415
ClinVar RCV Id: RCV000490432 RCV000455902 RCV001723786
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060004.3:p.Val805Ala
CA8391132
NM_017534.6:c.2414T>C