Canonical Allele Identifier: PA913194196
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 626816
ClinVar RCV Id: RCV000770481 RCV002533964
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Arg1050Gln
CA389045372
NM_000257.4:c.3149G>A