Canonical Allele Identifier: PA2825108836
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2069103
ClinVar RCV Id: RCV002961900
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Asn187His
CA389052551
NM_000257.4:c.559A>C