Canonical Allele Identifier: PA1139673776
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 921353
ClinVar RCV Id: RCV001180706 RCV001528519
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Lys1043Arg
CA389045444
NM_000257.4:c.3128A>G