Canonical Allele Identifier: PA2825109749
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2011800
ClinVar RCV Id: RCV002838679
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Gly414Arg
CA389051054
NM_000257.4:c.1240G>C
CA389051055
NM_000257.4:c.1240G>A