Canonical Allele Identifier: PA180513
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 36642
ClinVar RCV Id: RCV000030320 RCV000223711 RCV000199234 RCV000586653 RCV001170487 RCV000995812 RCV001251032 RCV002504832
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Arg1712Gln
CA015727
NM_000257.4:c.5135G>A