Canonical Allele Identifier: PA645414682
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 237443
ClinVar RCV Id: RCV000228376
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ile221Thr
CA10583173
NM_000257.4:c.662T>C