Canonical Allele Identifier: PA1139675130
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 926457
ClinVar RCV Id: RCV001189054 RCV001204564
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Glu1638Lys
CA389037370
NM_000257.4:c.4912G>A