Canonical Allele Identifier: PA2825540556
Gene: MYH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 445951
ClinVar RCV Id: RCV000513939 RCV000764101
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001093582.1:p.Ala1708Thr
CA8390487
NM_001100112.2:c.5122G>A