Canonical Allele Identifier: PA132143
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 43108
ClinVar RCV Id: RCV000036006
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ala279Thr
CA016872
NM_000257.4:c.835G>A