Canonical Allele Identifier: PA296578
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 181207
ClinVar RCV Id: RCV000158577 RCV000790958 RCV001187170 RCV001313026 RCV002478478 RCV002433702 RCV003320119 RCV004528897
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Glu935Val
CA013125
NM_000257.4:c.2804A>T