Canonical Allele Identifier: PA098831
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 164395
ClinVar RCV Id: RCV000766407 RCV000989193 RCV000845527 RCV001177617 RCV001307728 RCV002354346
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Pro211Leu
CA016570
NM_000257.4:c.632C>T