Canonical Allele Identifier: PA2825112669
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2006385
ClinVar RCV Id: RCV002811722
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ala1406Ser
CA389040470
NM_000257.4:c.4216G>T