Canonical Allele Identifier: PA1139673763
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 859822
ClinVar RCV Id: RCV001066016
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Val1031Ala
CA389045641
NM_000257.4:c.3092T>C