Canonical Allele Identifier: PA1139673613
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 925464
ClinVar RCV Id: RCV001187431
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Arg941Cys
CA389046936
NM_000257.4:c.2821C>T