Canonical Allele Identifier: PA180817
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 177821
ClinVar RCV Id: RCV000154454

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Phe468Leu
CA010692
NM_000257.4:c.1402T>C
CA389050696
NM_000257.4:c.1404C>A
CA389050697
NM_000257.4:c.1404C>G