Canonical Allele Identifier: PA1139675077
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 943200
ClinVar RCV Id: RCV001213343 RCV001797828 RCV001806051
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Arg1588Cys
CA389037681
NM_000257.4:c.4762C>T