Canonical Allele Identifier: PA296882
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 181380
ClinVar RCV Id: RCV000158855 RCV000226190 RCV000223789 RCV002433705
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Asp953Val
CA013157
NM_000257.4:c.2858A>T