Canonical Allele Identifier: PA1139673518
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 918407
ClinVar RCV Id: RCV001175977
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ile913Val
CA389047220
NM_000257.4:c.2737A>G