Canonical Allele Identifier: PA2499230335
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1018988
ClinVar RCV Id: RCV001318361 RCV003166841 RCV004005093
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Glu972Asp
CA257818865
NM_000257.4:c.2916G>C
CA389046599
NM_000257.4:c.2916G>T