Canonical Allele Identifier: PA658662865
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 454342
ClinVar RCV Id: RCV000554576 RCV004545785
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Phe494Tyr
CA389050501
NM_000257.4:c.1481T>A