Canonical Allele Identifier: PA2825112103
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2872849
ClinVar RCV Id: RCV003748017
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Gly984Arg
CA389046444
NM_000257.4:c.2950G>A
CA389046445
NM_000257.4:c.2950G>C