Canonical Allele Identifier: PA131812
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 42886
ClinVar RCV Id: RCV000035773 RCV000148962 RCV000628894 RCV001092198 RCV001110427 RCV001110428 RCV002415463 RCV003320052
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Arg723His
CA011859
NM_000257.4:c.2168G>A