Canonical Allele Identifier: PA2825108853
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2091614
ClinVar RCV Id: RCV002991657
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Tyr194Cys
CA389052488
NM_000257.4:c.581A>G