Canonical Allele Identifier: PA296762
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 181307
ClinVar RCV Id: RCV000223786 RCV000766401 RCV001191621 RCV001369678 RCV002498789 RCV004535032
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Met165Val
CA015475
NM_000257.4:c.493A>G