Canonical Allele Identifier: PA645414666
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 234643
ClinVar RCV Id: RCV000223475 RCV001191616 RCV003748210
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Val191Asp
CA10577510
NM_000257.4:c.572T>A