Canonical Allele Identifier: PA2573269797
Gene: MYH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1401309
ClinVar RCV Id: RCV001906267
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060004.3:p.Met360Leu
CA287745464
NM_017534.6:c.1078A>T
CA398163050
NM_017534.6:c.1078A>C