Canonical Allele Identifier: PA1139671933
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 952091
ClinVar RCV Id: RCV001224137
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Val273Phe
CA389051978
NM_000257.4:c.817G>T