Canonical Allele Identifier: PA131981
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 43002
ClinVar RCV Id: RCV000035896 RCV000700637 RCV003298056
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.His1419Arg
CA014711
NM_000257.4:c.4256A>G