Canonical Allele Identifier: PA2573166434
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1407759
ClinVar RCV Id: RCV001918605
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Met435Arg
CA389050906
NM_000257.4:c.1304T>G