Canonical Allele Identifier: PA915957407
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 658169
ClinVar RCV Id: RCV000814934
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ala1400Asp
CA389040533
NM_000257.4:c.4199C>A