Canonical Allele Identifier: PA296907
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 181393
ClinVar RCV Id: RCV000158869 RCV000799550 RCV001176078 RCV001293063 RCV002498790 RCV002336365 RCV004528899
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Arg1677His
CA015595
NM_000257.4:c.5030G>A