Canonical Allele Identifier: PA913194195
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 626818
ClinVar RCV Id: RCV000770483
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Met1046Val
CA389045419
NM_000257.4:c.3136A>G