Canonical Allele Identifier: PA180583
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 177656
ClinVar RCV Id: RCV000154244 RCV001207060
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Glu903Gly
CA012900
NM_000257.4:c.2708A>G