Canonical Allele Identifier: PA915957087
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 648360
ClinVar RCV Id: RCV000803073
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ile913Met
CA389047213
NM_000257.4:c.2739T>G