Canonical Allele Identifier: PA645416125
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 391904
ClinVar RCV Id: RCV000584770 RCV000428391 RCV001180607 RCV002446751 RCV003319198
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Arg807His
CA032556
NM_000257.4:c.2420G>A