Canonical Allele Identifier: PA296920
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 181401
ClinVar RCV Id: RCV000158881 RCV000225905 RCV000507832 RCV000620575
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Phe247Cys
CA016752
NM_000257.4:c.740T>G