Canonical Allele Identifier: PA2825108884
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1752372
ClinVar RCV Id: RCV003098175 RCV002366605
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Asp208Val
CA389052402
NM_000257.4:c.623A>T