Canonical Allele Identifier: PA2573166298
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1353468
ClinVar RCV Id: RCV001885533
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ile248Met
CA389052136
NM_000257.4:c.744T>G