Canonical Allele Identifier: PA351722
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 222722
ClinVar RCV Id: RCV000208036 RCV001323678 RCV001555393 RCV002390559 RCV003997685
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Glu466Lys
CA351720
NM_000257.4:c.1396G>A