Canonical Allele Identifier: PA097686
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 164350
ClinVar RCV Id: RCV000461116 RCV000770495 RCV000620591 RCV000766426 RCV001197245 RCV001258093
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Arg671Cys
CA011560
NM_000257.4:c.2011C>T