Canonical Allele Identifier: PA237389
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 191729
ClinVar RCV Id: RCV000172046 RCV000819613 RCV003995670
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Asn1244His
CA014003
NM_000257.4:c.3730A>C