Canonical Allele Identifier: PA2825112241
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1730021
ClinVar RCV Id: RCV002326252
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ser1102Thr
CA389044394
NM_000257.4:c.3305G>C