Canonical Allele Identifier: PA2499230394
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1007904
ClinVar RCV Id: RCV001305162 RCV004005027
ClinVar Variation Id: 1721155
ClinVar RCV Id: RCV002300256 RCV004005606
ClinVar Variation Id: 2773945
ClinVar RCV Id: RCV003532707
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Met922Ile
CA034234
NM_000257.4:c.2766G>T
CA257818961
NM_000257.4:c.2766G>A
CA389047129
NM_000257.4:c.2766G>C