Canonical Allele Identifier: PA2825112465
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 3071938
ClinVar RCV Id: RCV004011968
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Leu1252Trp
CA389042752
NM_000257.4:c.3755T>G