Canonical Allele Identifier: PA891844932
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 576107
ClinVar RCV Id: RCV000698524 RCV004026447
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ile913Ser
CA389047218
NM_000257.4:c.2738T>G