Canonical Allele Identifier: PA915957126
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 636633
ClinVar RCV Id: RCV000788522 RCV001525515 RCV002535779
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Arg941His
CA034403
NM_000257.4:c.2822G>A