Canonical Allele Identifier: PA097962
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 164313
ClinVar RCV Id: RCV000158574 RCV000622071 RCV000527742
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Asp928Asn
CA013046
NM_000257.4:c.2782G>A