Canonical Allele Identifier: PA2825497227
Gene: PTCH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2626237
ClinVar RCV Id: RCV003382217
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001077072.1:p.Ser1142Cys
CA374111695
NM_001083603.3:c.3425C>G