Canonical Allele Identifier: PA132100
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 43080
ClinVar RCV Id: RCV000035975 RCV004017303
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Glu1887Gly
CA016357
NM_000257.4:c.5660A>G