Canonical Allele Identifier: PA2825112224
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1729577
ClinVar RCV Id: RCV002445676
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ala1089Val
CA389044520
NM_000257.4:c.3266C>T