Canonical Allele Identifier: PA2825113133
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 3071432
ClinVar RCV Id: RCV004015926
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ile1627Ser
CA389037436
NM_000257.4:c.4880T>G