Canonical Allele Identifier: PA2825112221
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2858568
ClinVar RCV Id: RCV003747810
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Leu1087Val
CA389044546
NM_000257.4:c.3259C>G