Canonical Allele Identifier: PA645416630
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 426200
ClinVar RCV Id: RCV000490053 RCV000540550 RCV001184832 RCV003302724
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Glu1039Gly
CA035756
NM_000257.4:c.3116A>G