Canonical Allele Identifier: PA296559
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 181197
ClinVar RCV Id: RCV000158556 RCV001207169
ClinVar Variation Id: 582966
ClinVar RCV Id: RCV000707167 RCV001559101 RCV001798968
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Val878Leu
CA012769
NM_000257.4:c.2632G>C
CA389047937
NM_000257.4:c.2632G>T