Canonical Allele Identifier: PA097667
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 42875
ClinVar RCV Id: RCV000035758 RCV000158822 RCV000162333 RCV000168409 RCV000253409 RCV000477919 RCV000678721 RCV000762924 RCV001170503 RCV004534737
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Arg663His
CA011552
NM_000257.4:c.1988G>A