Canonical Allele Identifier: PA2580112199
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1694093
ClinVar RCV Id: RCV002261962
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ala1441_Leu1442insPro
CA2580088005
NM_000257.4:c.4322_4324dup