Canonical Allele Identifier: PA658804515
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 524986
ClinVar RCV Id: RCV000628930

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Val1430del
CA658798184
NM_000257.4:c.4289_4291del