Canonical Allele Identifier: PA1139673909
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 922231
ClinVar RCV Id: RCV001182163
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Leu1111Phe
CA389044302
NM_000257.4:c.3331C>T