Canonical Allele Identifier: PA645416678
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 418362
ClinVar RCV Id: RCV000700691 RCV003372725 RCV002496850 RCV002525769 RCV004002249
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Glu1056Asp
CA036012
NM_000257.4:c.3168G>C
CA389045324
NM_000257.4:c.3168G>T