Canonical Allele Identifier: PA097823
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 177667
ClinVar RCV Id: RCV000458948 RCV000587299 RCV000709745 RCV000845415 RCV001189960 RCV002426734 RCV002498735
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Arg869His
CA012723
NM_000257.4:c.2606G>A