Canonical Allele Identifier: PA2825111931
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1795958
ClinVar RCV Id: RCV002441332
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Asp928Gly
CA389047071
NM_000257.4:c.2783A>G