Canonical Allele Identifier: PA181007
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 177921
ClinVar RCV Id: RCV000154581 RCV000766422 RCV001054042 RCV001798499 RCV002390345
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Asp469Asn
CA010701
NM_000257.4:c.1405G>A