Canonical Allele Identifier: PA337502
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 216362
ClinVar RCV Id: RCV000197853 RCV002381688
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Met435Ile
CA337500
NM_000257.4:c.1305G>A
CA389050904
NM_000257.4:c.1305G>T
CA389050905
NM_000257.4:c.1305G>C