Canonical Allele Identifier: PA2499230284
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 978739
ClinVar RCV Id: RCV001293117

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ala1603Val
CA389037593
NM_000257.4:c.4808C>T