Canonical Allele Identifier: PA177060
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 164407
ClinVar RCV Id: RCV000151316 RCV001093026 RCV001185781 RCV001338885 RCV002345473
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Arg17His
CA015673
NM_000257.4:c.50G>A