Canonical Allele Identifier: PA645416568
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 407201
ClinVar RCV Id: RCV000458807 RCV001178873 RCV002510896
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Arg941Ser
CA034383
NM_000257.4:c.2821C>A