Canonical Allele Identifier: PA2499230337
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1011193
ClinVar RCV Id: RCV001308955 RCV002437053 RCV002504471
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Leu1010Phe
CA035267
NM_000257.4:c.3028C>T