Canonical Allele Identifier: PA296662
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 181252
ClinVar RCV Id: RCV000158649 RCV003748197
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Glu1424Lys
CA014734
NM_000257.4:c.4270G>A