Canonical Allele Identifier: PA658804500
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 505287
ClinVar RCV Id: RCV000604054
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Lys1294del
CA658798188
NM_000257.4:c.3880_3882del