Canonical Allele Identifier: PA1139674924
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 838150
ClinVar RCV Id: RCV001039638 RCV001799031 RCV002481873
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Glu1548Val
CA389037958
NM_000257.4:c.4643A>T