Canonical Allele Identifier: PA2825365149
Gene: HNRNPH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2577964
ClinVar RCV Id: RCV003325370
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001027565.1:p.Arg212Ser
CA413942627
NM_001032393.3:c.636G>C
CA413942628
NM_001032393.3:c.636G>T