Canonical Allele Identifier: PA915957157
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 810738
ClinVar RCV Id: RCV000999572
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Lys1022Glu
CA389045738
NM_000257.4:c.3064A>G