Canonical Allele Identifier: PA645414716
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 237444
ClinVar RCV Id: RCV000231604
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ala254Glu
CA10583172
NM_000257.4:c.761C>A