Canonical Allele Identifier: PA131856
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 42913
ClinVar RCV Id: RCV000143922 RCV000168354 RCV000201461 RCV000223913 RCV000248308 RCV001251000
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Lys847del
CA012568
NM_000257.4:c.2539_2541del