Canonical Allele Identifier: PA2825112355
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 3070067
ClinVar RCV Id: RCV004010099
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.His1185Gln
CA389043493
NM_000257.4:c.3555C>A
CA389043495
NM_000257.4:c.3555C>G