Canonical Allele Identifier: PA181045
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 177945
ClinVar RCV Id: RCV000154606 RCV000172042 RCV000470391 RCV001112386 RCV001112385 RCV001184477 RCV001112388 RCV003320111 RCV002336317 RCV004532746
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Arg1606Cys
CA015344
NM_000257.4:c.4816C>T