Canonical Allele Identifier: PA891844877
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 575443
ClinVar RCV Id: RCV000697662
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Asp382Gly
CA389051250
NM_000257.4:c.1145A>G