Canonical Allele Identifier: PA658804552
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 518640
ClinVar RCV Id: RCV000620963 RCV001327837 RCV003150309 RCV002510931
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Lys1919Asn
CA389034536
NM_000257.4:c.5757G>T
CA389034537
NM_000257.4:c.5757G>C