Canonical Allele Identifier: PA2825112232
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 3070918
ClinVar RCV Id: RCV004014420
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ile1094Thr
CA389044475
NM_000257.4:c.3281T>C