Canonical Allele Identifier: PA296660
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 181250
ClinVar RCV Id: RCV000158645 RCV001214464
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ser1413Leu
CA014687
NM_000257.4:c.4238C>T