Canonical Allele Identifier: PA212687
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 42860
ClinVar RCV Id: RCV000035741 RCV000799659 RCV003298054 RCV003223608 RCV003486554
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Arg567His
CA011148
NM_000257.4:c.1700G>A