Canonical Allele Identifier: PA2825113770
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 3070702
ClinVar RCV Id: RCV004013212
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Lys1895Arg
CA257807584
NM_000257.4:c.5684A>G