Canonical Allele Identifier: PA177054
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 164392
ClinVar RCV Id: RCV000599626 RCV002381471
ClinVar Variation Id: 571159
ClinVar RCV Id: RCV000692213 RCV002386201
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Phe247Leu
CA016744
NM_000257.4:c.739T>C
CA389052141
NM_000257.4:c.741C>G
CA389052142
NM_000257.4:c.741C>A