Canonical Allele Identifier: PA658804418
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 505562
ClinVar RCV Id: RCV000614191
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Arg403Gly
CA389051122
NM_000257.4:c.1207C>G