Canonical Allele Identifier: PA891844859
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 573829
ClinVar RCV Id: RCV000695599
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Gln193Leu
CA389052495
NM_000257.4:c.578A>T