Canonical Allele Identifier: PA296826
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 181345
ClinVar RCV Id: RCV001721010
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ile467Thr
CA010686
NM_000257.4:c.1400T>C