Canonical Allele Identifier: PA915957200
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 658282
ClinVar RCV Id: RCV000815076 RCV002487790 RCV004001771 RCV004028837
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Asp1077Tyr
CA036217
NM_000257.4:c.3229G>T