Canonical Allele Identifier: PA180671
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 177734
ClinVar RCV Id: RCV000154344 RCV000469589 RCV002415654
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Pro710His
CA011747
NM_000257.4:c.2129C>A