Canonical Allele Identifier: PA097599
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 14088
ClinVar RCV Id: RCV000015144 RCV000229956 RCV000158761 RCV000617265 RCV000762925 RCV000853263
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Arg249Gln
CA016781
NM_000257.4:c.746G>A