Canonical Allele Identifier: PA913194328
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 617741
ClinVar RCV Id: RCV000754866
ClinVar Variation Id: 626537
ClinVar RCV Id: RCV000769434
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Met1730Ile
CA389036754
NM_000257.4:c.5190G>T
CA389036755
NM_000257.4:c.5190G>C
CA389036756
NM_000257.4:c.5190G>A