Canonical Allele Identifier: PA296567
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 181201
ClinVar RCV Id: RCV000158563 RCV001857567
ClinVar Variation Id: 1038786
ClinVar RCV Id: RCV001342138
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Asp900Glu
CA012887
NM_000257.4:c.2700T>A
CA389047343
NM_000257.4:c.2700T>G