Canonical Allele Identifier: PA2573166432
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1388917
ClinVar RCV Id: RCV001886903
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Lys429Glu
CA389050951
NM_000257.4:c.1285A>G