Canonical Allele Identifier: PA658804490
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 525014
ClinVar RCV Id: RCV000628979
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Glu1070Val
CA389045189
NM_000257.4:c.3209A>T