Canonical Allele Identifier: PA097776
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 42900
ClinVar RCV Id: RCV000035789 RCV000148708 RCV000250929 RCV000313839 RCV000348947 RCV000354671 RCV000392220 RCV000584813 RCV000776332 RCV001705651 RCV003320055
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Arg787His
CA012239
NM_000257.4:c.2360G>A