Canonical Allele Identifier: PA2825492294
Gene: PTCH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1753216
ClinVar RCV Id: RCV002354092

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001077072.1:p.Thr212Arg
CA374115044
NM_001083603.3:c.635C>G