Canonical Allele Identifier: PA891852785
Gene: MYH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 585068
ClinVar RCV Id: RCV000709832 RCV001063613
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060004.3:p.Ala870Val
CA398145279
NM_017534.6:c.2609C>T