Canonical Allele Identifier: PA131989
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 43008
ClinVar RCV Id: RCV000035902

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Lys1444Glu
CA014823
NM_000257.4:c.4330A>G