Canonical Allele Identifier: PA2499230269
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1025672
ClinVar RCV Id: RCV001326014

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Arg1114Pro
CA389044212
NM_000257.4:c.3341G>C