Canonical Allele Identifier: PA2573165107
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1475638
ClinVar RCV Id: RCV002007920 RCV003170300
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Gln1075His
CA389045119
NM_000257.4:c.3225G>T
CA389045120
NM_000257.4:c.3225G>C