Canonical Allele Identifier: PA180627
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 177692
ClinVar RCV Id: RCV000158746 RCV000706637 RCV002354363
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ala199Val
CA016513
NM_000257.4:c.596C>T