Canonical Allele Identifier: PA1139674929
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 852384
ClinVar RCV Id: RCV001056980
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Glu1552Asp
CA043403
NM_000257.4:c.4656G>T
CA389037921
NM_000257.4:c.4656G>C