Canonical Allele Identifier: PA645416698
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 407167
ClinVar RCV Id: RCV000460286
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Glu1095Lys
CA036626
NM_000257.4:c.3283G>A