Canonical Allele Identifier: PA2825111132
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2577034
ClinVar RCV Id: RCV003324112
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Thr761Ile
CA389048746
NM_000257.4:c.2282C>T