Canonical Allele Identifier: PA915956746
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 644099
ClinVar RCV Id: RCV000797940 RCV002386408
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Gly458Val
CA389050759
NM_000257.4:c.1373G>T