Canonical Allele Identifier: PA658804532
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 519197
ClinVar RCV Id: RCV000617490
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ala1632Asp
CA389037403
NM_000257.4:c.4895C>A