Canonical Allele Identifier: PA915957417
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 650679
ClinVar RCV Id: RCV000805875 RCV002290449 RCV003532272 RCV004538104
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Phe1449Leu
CA389040001
NM_000257.4:c.4347C>G
CA389040002
NM_000257.4:c.4347C>A
CA389040009
NM_000257.4:c.4345T>C