Canonical Allele Identifier: PA132112
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 43088
ClinVar RCV Id: RCV000035983 RCV000132760 RCV000192205 RCV001329735 RCV002510774 RCV003149624 RCV002513365
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Glu1914Lys
CA016441
NM_000257.4:c.5740G>A