Canonical Allele Identifier: PA915957376
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 689588
ClinVar RCV Id: RCV000850345 RCV002363194 RCV002487879 RCV002536173 RCV003320763 RCV004002903
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Arg1289Gln
CA389041779
NM_000257.4:c.3866G>A