Canonical Allele Identifier: PA296922
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 181402
ClinVar RCV Id: RCV000158882 RCV000584771 RCV000536809 RCV001187174 RCV001270160
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Asp309Asn
CA016961
NM_000257.4:c.925G>A