Canonical Allele Identifier: PA1139674693
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 860786
ClinVar RCV Id: RCV001067157

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ala1441dup
CA916081707
NM_000257.4:c.4317_4319dup