Canonical Allele Identifier: PA097741
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 14095
ClinVar RCV Id: RCV000015151 RCV000158516 RCV000035772 RCV000253053 RCV001186219 RCV000462477 RCV002496365
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Arg723Cys
CA011851
NM_000257.4:c.2167C>T