Canonical Allele Identifier: PA132053
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 43049
ClinVar RCV Id: RCV000035943 RCV000148703 RCV001050756 RCV001184540 RCV001719728 RCV004018782
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Arg1662His
CA015524
NM_000257.4:c.4985G>A