Canonical Allele Identifier: PA132057
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 43051
ClinVar RCV Id: RCV000035945
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ala1672_Ile1673del
CA015559
NM_000257.4:c.5015_5020del