Canonical Allele Identifier: PA658659165
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 449317
ClinVar RCV Id: RCV000521554 RCV000688117 RCV002490901 RCV004003601
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ala1660Glu
CA257810052
NM_000257.4:c.4979C>A