Canonical Allele Identifier: PA2825110302
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 3015244
ClinVar RCV Id: RCV003870851
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Pro566Ala
CA389050010
NM_000257.4:c.1696C>G