Canonical Allele Identifier: PA915957503
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 662104
ClinVar RCV Id: RCV000819672 RCV001187948 RCV002336700
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ala1672Thr
CA044783
NM_000257.4:c.5014G>A