Canonical Allele Identifier: PA2825113443
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 3073600
ClinVar RCV Id: RCV004016606
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Glu1772Gln
CA389035864
NM_000257.4:c.5314G>C