Canonical Allele Identifier: PA2573165191
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1418212
ClinVar RCV Id: RCV001952003 RCV003533056
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Asn1664Ser
CA389037184
NM_000257.4:c.4991A>G