Canonical Allele Identifier: PA645416599
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 312904
ClinVar RCV Id: RCV000289515 RCV000311891 RCV000351443 RCV000348122 RCV000402174 RCV003995840 RCV003320164
ClinVar Variation Id: 665805
ClinVar RCV Id: RCV000824170
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ala990Thr
CA035008
NM_000257.4:c.2968G>A
CA915946996
NM_000257.4:c.2967_2968delinsCA